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GENE - TERM ANNOTATION REPORT

192 Annotations Found.

An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688089 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15556047 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623542 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20129283 PMID:22581653 PMID:24033266 PMID:25741868 PMID:25904541 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:151764941 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24529773 PMID:25741868 PMID:25904541 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623834 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:17438607 PMID:17438610 PMID:19841300 PMID:20129283 PMID:21185501 PMID:22581653 PMID:24033266 PMID:25741868 PMID:25904541 PMID:26332594 PMID:26746457 PMID:27566755 PMID:28492532 PMID:32048431 PMID:33500567 PMID:34935411


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623449 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16712702 PMID:18508782 PMID:19716085 PMID:22581653 PMID:23631430 PMID:25741868 PMID:25904541 PMID:28438721 PMID:28492532 PMID:31610692 PMID:34379075


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17805561


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Zhu W, etal., Circ Res. 2018 Dec 18. doi: 10.1161/CIRCRESAHA.118.314050.
  • 2 additional annotations were made from Zhu W, etal., Circ Res. 2018 Dec 18. doi: 10.1161/CIRCRESAHA.118.314050.
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Qualifier: treatment
  • Curation Notes: DNA:mutations:cds:


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28875167 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18368697 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Qualifier: susceptibility


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606766 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:26164358 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598300 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10590249 PMID:11889015


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611148 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:15992732 PMID:16453024 PMID:17331104 PMID:18378609 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23571586 PMID:23861362 PMID:24033266 PMID:25741868 PMID:26220391 PMID:26332594 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611152 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18088563 PMID:19026623 PMID:20875080 PMID:23098067 PMID:24033266 PMID:25741868 PMID:26467025 PMID:27554632 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598310 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11823453 PMID:12639704 PMID:15121794 PMID:15689442 PMID:15851227 PMID:15851440 PMID:15992732 PMID:16155735 PMID:16568155 PMID:16707561 PMID:17210839 PMID:17605181 PMID:17905336 PMID:18245395 PMID:18378609 PMID:18976777 PMID:19841300 PMID:20129283 PMID:20981092 PMID:22378279 PMID:22519808 PMID:22581653 PMID:22682427 PMID:23465283 PMID:23853484 PMID:23861362 PMID:24033266 PMID:24784157 PMID:25051102 PMID:25741868 PMID:26131924 PMID:26159999 PMID:26467025 PMID:27153395 PMID:28472724 PMID:28491758 PMID:28492532 PMID:28493952 PMID:28498465 PMID:28638671 PMID:29672598 PMID:29997009 PMID:30079003 PMID:30146492 PMID:30419068 PMID:8661019


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598311 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12193783 PMID:12471205 PMID:14500339 PMID:15161528 PMID:15851227 PMID:15992732 PMID:16061744 PMID:16453014 PMID:16453024 PMID:16731473 PMID:16922724 PMID:17185997 PMID:17275750 PMID:17892895 PMID:17967976 PMID:18362431 PMID:18378609 PMID:18452875 PMID:19302788 PMID:19305408 PMID:19305409 PMID:19841300 PMID:20129283 PMID:20403459 PMID:20470418 PMID:20486126 PMID:21325150 PMID:21385947 PMID:21498565 PMID:21621375 PMID:22581653 PMID:22984773 PMID:23091201 PMID:23861362 PMID:24033266 PMID:24332150 PMID:24951663 PMID:25065297 PMID:25741868 PMID:25757662 PMID:25923670 PMID:26467025 PMID:28492532 PMID:29431662 PMID:30364184


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603047 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25051102 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611149 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19026623 PMID:22984773 PMID:24033266 PMID:25741868 PMID:26159999 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611155 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23861362 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611175 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19841300 PMID:20129283 PMID:22581653 PMID:24033266 PMID:25351510 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611163 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19026623 PMID:20875080 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603044 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10508990 PMID:19666841 PMID:22984773 PMID:24033266 PMID:25051102 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611160 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10807545 PMID:15689442 PMID:15851227 PMID:16155735 PMID:17227473 PMID:18426444 PMID:19841300 PMID:20129283 PMID:21321465 PMID:22581653 PMID:23861362 PMID:24033266 PMID:24463578 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611178 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11710892 PMID:11960580 PMID:19026623 PMID:22984773 PMID:23098067 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603046 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10807545 PMID:11901046 PMID:14967853 PMID:15176425 PMID:15851227 PMID:15992732 PMID:15996170 PMID:16379539 PMID:17210839 PMID:17210841 PMID:17587741 PMID:18426444 PMID:19841300 PMID:20129283 PMID:20636320 PMID:21109022 PMID:21167004 PMID:22378279 PMID:22581653 PMID:22677073 PMID:22995991 PMID:23414114 PMID:23465283 PMID:23571586 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24317018 PMID:25637381 PMID:25741868 PMID:26467025 PMID:27153395 PMID:27381756 PMID:27711072 PMID:28087566 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611141 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11960580 PMID:11997281 PMID:15992732 PMID:17161064 PMID:17675083 PMID:17993325 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23861362 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623496 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12354768 PMID:12820704 PMID:15466642 PMID:15840476 PMID:16540748 PMID:17161064 PMID:17210839 PMID:18071069 PMID:18452873 PMID:19412328 PMID:20403459 PMID:20875080 PMID:22378279 PMID:22581653 PMID:23008441 PMID:23098067 PMID:24033266 PMID:24653702 PMID:25741868 PMID:26209461 PMID:26467025 PMID:26749013 PMID:27287068 PMID:28265756 PMID:28492532 PMID:28781330 PMID:29032884


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623823 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:25741868 PMID:25904541 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689342 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16453024 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606805 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692790 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:28725320


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692787 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19026623 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623525 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12566525 PMID:15851227 PMID:15998675 PMID:17905336 PMID:17908752 PMID:19322600 PMID:19841300 PMID:20129283 PMID:20403459 PMID:22378279 PMID:22581653 PMID:23465283 PMID:23861362 PMID:24033266 PMID:24055113 PMID:25351510 PMID:25637381 PMID:25741868 PMID:26159999 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603042 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:14760488 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603048 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:17210839 PMID:17210841 PMID:18378609 PMID:19027780 PMID:19412328 PMID:19841300 PMID:20129283 PMID:21705349 PMID:22378279 PMID:22581653 PMID:22685113 PMID:22840528 PMID:23299917 PMID:23414114 PMID:23465283 PMID:24033266 PMID:24667783 PMID:24721456 PMID:24721642 PMID:25554238 PMID:25741868 PMID:26159999 PMID:26406308 PMID:26743238 PMID:27287068 PMID:27435932 PMID:28087566 PMID:28492532 PMID:31043699


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623837 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10961955 PMID:15851227 PMID:16379539 PMID:16712702 PMID:17210839 PMID:17210841 PMID:19412328 PMID:19597050 PMID:19841298 PMID:19841300 PMID:20102864 PMID:20129283 PMID:20875080 PMID:2107088 PMID:21070882 PMID:21109022 PMID:21410720 PMID:22378279 PMID:22581653 PMID:22677073 PMID:23465283 PMID:23571586 PMID:23631430 PMID:23714088 PMID:24033266 PMID:24606995 PMID:25741868 PMID:26159999 PMID:26746457 PMID:27153395 PMID:28301460 PMID:28492532 PMID:28831623 PMID:29672598 PMID:31043699


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692797 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10508990 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611177 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:17210839 PMID:17210841 PMID:17605181 PMID:18071069 PMID:18456723 PMID:19406494 PMID:19841300 PMID:20129283 PMID:22581653 PMID:22685113 PMID:23414114 PMID:23465283 PMID:23861362 PMID:23936059 PMID:24033266 PMID:25410959 PMID:25741868 PMID:26159999 PMID:26467025 PMID:27711072 PMID:28359509 PMID:28492532 PMID:29449963 PMID:29672598 PMID:31337358 PMID:32470535


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9688084 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19026623 PMID:21596231 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598318 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12522116 PMID:15466643 PMID:15671429 PMID:15998690 PMID:16684018 PMID:19251209 PMID:20129283 PMID:20384651 PMID:20539757 PMID:21596231 PMID:21824921 PMID:22247482 PMID:22581653 PMID:23791817 PMID:24136861 PMID:24573164 PMID:24762805 PMID:25741868 PMID:26111534 PMID:28492532 PMID:28637969 PMID:33131149 PMID:3953067


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057252 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16199547 PMID:20129283 PMID:22789973 PMID:23631430 PMID:24033266 PMID:25741868 PMID:28341781 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623831 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23861362 PMID:24033266 PMID:25741868 PMID:25904541 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623583 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:25741868 PMID:26129877 PMID:28492532 PMID:29167113


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11586315 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15996170 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623847 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11901046 PMID:20129283 PMID:22581653 PMID:24033266 PMID:25741868 PMID:25829473 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623835 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19716085 PMID:22581653 PMID:23382499 PMID:24631775 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8692802 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18849657 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598313 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11748104 PMID:14523039 PMID:19251209 PMID:20031634 PMID:20129283 PMID:20539757 PMID:22581653 PMID:25741868 PMID:28492532 PMID:30662450


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623472 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:16712702 PMID:18378609 PMID:18508782 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23861362 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623746 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10973849 PMID:15840476 PMID:19716085 PMID:22581653


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057265 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:28492532 PMID:29544605


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13534778 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:26173111 PMID:26746457 PMID:27707468 PMID:28492532 PMID:29306897 PMID:29447731 PMID:30847666 PMID:32533946 PMID:32880476 PMID:34426522 PMID:34621001


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10408718 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24631775 PMID:25741868 PMID:28492532 PMID:34008892


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057323 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:23631430 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29907895


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623846 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12574143 PMID:16922724 PMID:20031634 PMID:22581653 PMID:24631775 PMID:24815523 PMID:25741868 PMID:28492532 PMID:28779003 PMID:29247119 PMID:31696929 PMID:32893267 PMID:33071830 PMID:35284542 PMID:35701104


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598314 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:14523039 PMID:15671429 PMID:17368591 PMID:20129283 PMID:20384651 PMID:20448214 PMID:20539757 PMID:21273195 PMID:21596231 PMID:22581653 PMID:22677073 PMID:22685113 PMID:23414114 PMID:23571586 PMID:24033266 PMID:24055113 PMID:24059039 PMID:24136861 PMID:24613995 PMID:24762805 PMID:24784157 PMID:25171853 PMID:25351510 PMID:25637381 PMID:25741868 PMID:26636822 PMID:26743238 PMID:26884609 PMID:27066507 PMID:27332903 PMID:28492532 PMID:31337358 PMID:31737537 PMID:32048431


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:153000470 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:31737537


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623840 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19406494 PMID:19716085 PMID:22581653 PMID:25741868 PMID:25904541 PMID:28492532 PMID:30847666 PMID:31737537 PMID:32893267


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623646 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11901046 PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:22885917 PMID:23321620 PMID:23414114 PMID:23861362 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623602 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19716085 PMID:22581653 PMID:24055113 PMID:24631775 PMID:25637381 PMID:25741868 PMID:25904541 PMID:26332594 PMID:28492532 PMID:32009526 PMID:32449611


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11350249 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:28492532 PMID:30690642


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623670 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20129283 PMID:22581653 PMID:235469 PMID:24136861 PMID:25741868 PMID:28074886 PMID:28492532 PMID:29540472 PMID:30086531 PMID:31737537 PMID:32533946 PMID:32880476 PMID:32893267 PMID:33221895 PMID:33996946 PMID:36516610 PMID:36724992


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623827 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18378609 PMID:21321465 PMID:22581653 PMID:22685113 PMID:25741868 PMID:28202948 PMID:28492532 PMID:32048431 PMID:36129056


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623587 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19841300 PMID:20129283 PMID:22581653 PMID:25741868 PMID:25904541 PMID:26746457 PMID:28492532 PMID:30079003


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623651 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12106943 PMID:17854786 PMID:19251209 PMID:19843921 PMID:20129283 PMID:20646679 PMID:21273195 PMID:22373669 PMID:22581653 PMID:22885917 PMID:23414114 PMID:24033266 PMID:24400668 PMID:24573164 PMID:24951569 PMID:25179549 PMID:25741868 PMID:25904541 PMID:26743238 PMID:28492532 PMID:28790152 PMID:291807 PMID:29759671 PMID:30059973 PMID:30609406 PMID:30662450 PMID:30847666 PMID:32893267 PMID:36516610 PMID:37061847


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623717 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10973849 PMID:19027780 PMID:19716085 PMID:19841300 PMID:20102864 PMID:20129283 PMID:21185501 PMID:22331908 PMID:22581653 PMID:22840528 PMID:23631430 PMID:24136861 PMID:24573164 PMID:24721456 PMID:25741868 PMID:28492532 PMID:28494446 PMID:29606593 PMID:29956481 PMID:30059973 PMID:30193851 PMID:30369311 PMID:31447099 PMID:32533187 PMID:33221895 PMID:34135346


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623470 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:24033266 PMID:25351510 PMID:25649125 PMID:25741868 PMID:25904541 PMID:28301460 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13486645 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32009526


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057200 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:27554632 PMID:28492532 PMID:28878402 PMID:34678660


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623711 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19167345 PMID:19716085 PMID:22581653 PMID:23174487 PMID:23631430 PMID:23861362 PMID:25741868 PMID:28492532 PMID:31231243 PMID:32893267 PMID:33712541 PMID:34758253


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13796157 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31737537


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623780 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12639704 PMID:15023552 PMID:20129283 PMID:21126620 PMID:22581653 PMID:22840528 PMID:22984773 PMID:23420830 PMID:25741868 PMID:25904541 PMID:26111534 PMID:28341781 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598292 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:14523039 PMID:15840483 PMID:16325048 PMID:18361072 PMID:20129283 PMID:20539757 PMID:25741868 PMID:25829473 PMID:26187847 PMID:28069705 PMID:28341781 PMID:28492532 PMID:29574140 PMID:32600061 PMID:33221895


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:38499785 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:26746457 PMID:27711072 PMID:28492532 PMID:30079003 PMID:30662450


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057338 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11562792 PMID:25741868


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12882069 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:17897635 PMID:18361072 PMID:22899775 PMID:25741868 PMID:27207958 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057321 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:22360817 PMID:24033266 PMID:25741868 PMID:25904541 PMID:27566755 PMID:28323875 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13813276 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:27871843 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623606 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19841300 PMID:20129283 PMID:22581653 PMID:25741868 PMID:26467025 PMID:26746457 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057233 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:23098067 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13491215 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20129283 PMID:24033266 PMID:24136861 PMID:24613995 PMID:25741868 PMID:25904541 PMID:28492532 PMID:29748316 PMID:33500567 PMID:34930020


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611156 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10966831 PMID:16267253 PMID:16611632 PMID:19716085 PMID:19799913 PMID:20129283 PMID:21622575 PMID:22581653 PMID:23571586 PMID:24033266 PMID:24136861 PMID:24736382 PMID:25741868 PMID:28492532 PMID:30193851 PMID:30972196 PMID:32268277 PMID:32533946 PMID:32893267 PMID:33221895 PMID:34935411


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623585 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19716085 PMID:22581653 PMID:24033266 PMID:25741868 PMID:26633542 PMID:27077130 PMID:28492532 PMID:29420653 PMID:30847666


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623791 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15840476 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23805106 PMID:24033266 PMID:25351510 PMID:25741868 PMID:25904541 PMID:28492532 PMID:28600387 PMID:32048431


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623833 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15996170 PMID:18426444 PMID:20123697 PMID:22581653 PMID:24363352 PMID:25741868 PMID:26798387 PMID:27026747 PMID:27871843 PMID:28492532 PMID:28988457 PMID:29349559 PMID:30532816


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057188 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:36516610


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9689341 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:25904541 PMID:28492532 PMID:30847666


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13477588 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31737537 PMID:32145446 PMID:32880476


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057241 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:28492532 PMID:31776209


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598289 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10973849 PMID:14736542 PMID:15840476 PMID:17118339 PMID:17905336 PMID:19716085 PMID:19762097 PMID:19841300 PMID:22581653 PMID:28412158 PMID:28492532 PMID:7889574 PMID:8541846 PMID:8620612 PMID:8917568


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057293 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24895455 PMID:25741868 PMID:26282245 PMID:27650965 PMID:28069705 PMID:28492532 PMID:29907873 PMID:30662450 PMID:30847666 PMID:33083013


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11040338 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:26159999 PMID:26281194 PMID:28492532 PMID:32323320


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623798 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15840476 PMID:19716085 PMID:19841300 PMID:20129283 PMID:22378279 PMID:22581653 PMID:23174487 PMID:25351510 PMID:25741868 PMID:25904541 PMID:27566755 PMID:28416588 PMID:28492532 PMID:28567303 PMID:31638414


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623601 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:18451998 PMID:19841300 PMID:20129283 PMID:22581653 PMID:24529773 PMID:25741868 PMID:25904541 PMID:27707468 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:26903769 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:22840528 PMID:25741868 PMID:28492532 PMID:30662450


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057229 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:23631430 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13813139 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:21726068 PMID:25172307 PMID:25741868 PMID:25815641 PMID:25904541 PMID:28492532 PMID:28834665 PMID:30615648


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13606771 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29396561


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623824 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16267250 PMID:17854786 PMID:18508782 PMID:20129283 PMID:22581653 PMID:25741868 PMID:27816319 PMID:28492532 PMID:31534214 PMID:31983221 PMID:34461752


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598293 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11410597 PMID:14990510 PMID:15840476 PMID:16254012 PMID:16980337 PMID:18929331 PMID:19716085 PMID:19841300 PMID:22129298 PMID:22581653 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12885646 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:27485560 PMID:28492532 PMID:29895855


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623608 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18378609 PMID:21143119 PMID:22581653 PMID:24631775 PMID:25741868 PMID:25904541 PMID:28492532 PMID:29247119


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057206 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24613995 PMID:25741868 PMID:28492532 PMID:30847666


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057205 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29038103 PMID:30847666


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611151 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10807545 PMID:10807547 PMID:11463728 PMID:11997281 PMID:12569159 PMID:12639704 PMID:14760488 PMID:14985827 PMID:15161528 PMID:15599693 PMID:15689442 PMID:16132053 PMID:16155735 PMID:16239976 PMID:16712702 PMID:17161064 PMID:17210839 PMID:17675083 PMID:17993325 PMID:18093912 PMID:18156160 PMID:18362431 PMID:18426444 PMID:19083750 PMID:19841300 PMID:20129283 PMID:22581653 PMID:23861362 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13809587 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24981977 PMID:25741868 PMID:28492532 PMID:29544605


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13822381 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:27485560 PMID:28492532 PMID:30847666


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623838 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10961955 PMID:22581653 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057333 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30244407 PMID:31737537 PMID:32431610


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13468099 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:17576681 PMID:20129283 PMID:23874304 PMID:25741868 PMID:26332594 PMID:27711072 PMID:28492532 PMID:30662450 PMID:9536098


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598305 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11804990 PMID:19056759 PMID:22581653 PMID:24033266 PMID:25741868 PMID:28492532 PMID:31983221


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057203 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31696929


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623475 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:25741868 PMID:26771585 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623867 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11076825 PMID:11901046 PMID:21840964 PMID:22581653 PMID:24033266 PMID:25261036 PMID:25741868 PMID:28492532 PMID:31737537


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8604247 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19412328 PMID:19716085 PMID:20458009 PMID:21167004 PMID:21483645 PMID:21596231 PMID:22277643 PMID:22581653 PMID:22710484 PMID:22766342 PMID:22999724 PMID:24815523 PMID:25210054 PMID:25624448 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623763 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20609320 PMID:22581653 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057320 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:28492532 PMID:30662450 PMID:32233023


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583380 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:17438610 PMID:25741868 PMID:25904541 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623750 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20129283 PMID:21273195 PMID:22581653 PMID:24167619 PMID:25741868 PMID:28492532 PMID:33164571


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13529651 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:23424222 PMID:25741868 PMID:27810048 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598294 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10200053 PMID:10508990 PMID:10618304 PMID:10772658 PMID:10973849 PMID:12574983 PMID:15051636 PMID:15184283 PMID:15621041 PMID:15670972 PMID:16922724 PMID:19167409 PMID:19716085 PMID:19841300 PMID:19863579 PMID:20090423 PMID:20129283 PMID:22360817 PMID:22581653 PMID:24218437 PMID:25904541 PMID:28492532 PMID:9495298 PMID:9506831


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623591 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11960580 PMID:19716085 PMID:20129283 PMID:22581653 PMID:22739120 PMID:23321620 PMID:23805106 PMID:24136861 PMID:25741868 PMID:26680202 PMID:28492532 PMID:30193851 PMID:30476647 PMID:34122134


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11093017 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:33221895


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12900397 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:28341781 PMID:28492532 PMID:31470130 PMID:34219138


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623737 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19716085 PMID:21051419 PMID:22581653 PMID:22685113 PMID:23631430 PMID:23838598 PMID:24033266 PMID:24144883 PMID:24606995 PMID:25051102 PMID:25741868 PMID:25904541 PMID:26213684 PMID:27153395 PMID:28492532 PMID:28988457 PMID:29396561 PMID:30847666 PMID:31737537 PMID:31983221 PMID:9716085


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598307 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11710892 PMID:18378609 PMID:19716085 PMID:22581653 PMID:23465283 PMID:24033266 PMID:24055113 PMID:25637381 PMID:25741868 PMID:27077130 PMID:28492532 PMID:29540853 PMID:30079003 PMID:31657683


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Scn5a (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: OMIM:603830


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10046736 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19706159 PMID:25741868 PMID:25904541 PMID:28492532 PMID:31983221


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623464 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10961955 PMID:15840476 PMID:16712702 PMID:19716085 PMID:21193062 PMID:22581653 PMID:22721569 PMID:23098067 PMID:23158531 PMID:24709866 PMID:25741868 PMID:26888838 PMID:27041150 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057339 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:23631430 PMID:25741868 PMID:28492532 PMID:32048431


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611154 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15840476 PMID:19412328 PMID:19841300 PMID:20129283 PMID:22337857 PMID:22581653 PMID:23631430 PMID:24033266 PMID:24613995 PMID:25741868 PMID:25904541 PMID:26633542 PMID:28150151 PMID:28492532 PMID:28600387 PMID:28807990 PMID:29728395 PMID:29884292 PMID:30079003 PMID:30193851 PMID:31737537 PMID:32048431 PMID:32091595 PMID:33131149 PMID:34426522


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9832518 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:26820365 PMID:28492532 PMID:32893267 PMID:33221895 PMID:36516610


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623845 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12574143 PMID:16922724 PMID:19251209 PMID:19606473 PMID:19716085 PMID:20031634 PMID:20129283 PMID:22581653 PMID:22885917 PMID:24136861 PMID:24573164 PMID:24815523 PMID:25624448 PMID:25637381 PMID:25741868 PMID:26022185 PMID:26916278 PMID:28449774 PMID:28492532 PMID:29167113 PMID:29728395 PMID:30193851 PMID:30847666 PMID:31447099 PMID:31866066 PMID:31981491 PMID:32048431 PMID:32746448 PMID:32893267 PMID:33131149 PMID:34620408 PMID:36516610


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623527 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20129283 PMID:22581653 PMID:24573164 PMID:25741868 PMID:28492532 PMID:29728395 PMID:30847666


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623446 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11823453 PMID:12106943 PMID:14687250 PMID:15028074 PMID:19251209 PMID:19716085 PMID:20129283 PMID:21273195 PMID:22373669 PMID:22581653 PMID:22885917 PMID:24033266 PMID:24136861 PMID:25741868 PMID:26538325 PMID:28341588 PMID:28492532 PMID:28600387 PMID:32533946


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623582 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16712702 PMID:19841300 PMID:19862833 PMID:20102864 PMID:22581653 PMID:24033266 PMID:24055113 PMID:25637381 PMID:25741868 PMID:25904541 PMID:26746457 PMID:27000522 PMID:28492532 PMID:32880476 PMID:33906374


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623485 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19716085 PMID:22581653 PMID:24349418 PMID:25741868 PMID:25904541 PMID:26746457 PMID:28492532 PMID:28549997 PMID:28573431 PMID:34843967


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623631 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11901046 PMID:22581653 PMID:25741868 PMID:25904541 PMID:28492532 PMID:30891416


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens) & RGD:11583144|RGD:11586388|RGD:13462196|RGD:13796140|RGD:13796174|RGD:13827599|RGD:14692400|RGD:14698124|RGD:14698125|RGD:15015378|RGD:15015380|RGD:28869278|RGD:34897778|RGD:405270486 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens) & RGD:10057258|RGD:10057275|RGD:10057289|RGD:11346043|RGD:11349571|RGD:11543745|RGD:11546864|RGD:11582340|RGD:11583585|RGD:11585051|RGD:11585869|RGD:11586354|RGD:11586373|RGD:11645808|RGD:126743212|RGD:127279906|RGD:127314414|RGD:12740763|RGD:12838724|RGD:12847003|RGD:12847153|RGD:12847460|RGD:13469925|RGD:13495337|RGD:13526469|RGD:13535095|RGD:13592608|RGD:13796172|RGD:13817878|RGD:14692544|RGD:14694156|RGD:150453134|RGD:15121900|RGD:15130077|RGD:21068524|RGD:26887692|RGD:34901666|RGD:38462355|RGD:38481371|RGD:8692777|RGD:8692788|RGD:8692789|RGD:9832514 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623545 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15671429 PMID:17442746 PMID:18048769 PMID:22581653 PMID:23321620 PMID:24033266 PMID:24815523 PMID:256650 PMID:25741868 PMID:26669661 PMID:26733869 PMID:28341781 PMID:28492532 PMID:30662450 PMID:30847666 PMID:30975432 PMID:31447099 PMID:31983221 PMID:32389048 PMID:32533946 PMID:32659924 PMID:32893267 PMID:33131149 PMID:33221895 PMID:34147702 PMID:34461752 PMID:36291626 PMID:8972392


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623615 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15996170 PMID:19996378 PMID:22581653 PMID:24033266 PMID:25741868 PMID:26632536 PMID:26743238 PMID:28472724 PMID:28492532 PMID:29202755 PMID:30165862 PMID:31983221


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13480511 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30122538 PMID:33029862 PMID:34555931 PMID:35124229 PMID:37061847


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057290 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15840476 PMID:19862833 PMID:23936059 PMID:24388587 PMID:25741868 PMID:27532257 PMID:28370132 PMID:28492532 PMID:28600387 PMID:29396561 PMID:29961767 PMID:31447099 PMID:32533946 PMID:33087929 PMID:36129056


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057315 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10448858 PMID:14654377 PMID:18697752 PMID:20728579 PMID:23098067 PMID:26022185 PMID:26467377 PMID:28492532 PMID:7651517 PMID:7889574


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:14691073 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:14985827 PMID:22984773 PMID:25741868 PMID:28492532 PMID:30662450 PMID:33221895 PMID:34649698


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598295 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10377081 PMID:10727653 PMID:10961955 PMID:10973849 PMID:11901046 PMID:12877697 PMID:15840476 PMID:16379539 PMID:18451998 PMID:18452873 PMID:18508782 PMID:19716085 PMID:19841300 PMID:20129283 PMID:21321465 PMID:22581653 PMID:23631430 PMID:24033266 PMID:24439875 PMID:24762805 PMID:24784157 PMID:24871449 PMID:25741868 PMID:26125038 PMID:27381756 PMID:27566755 PMID:28492532 PMID:28781849 PMID:29806494 PMID:30385166 PMID:31447099 PMID:31737537 PMID:32096284 PMID:32533946 PMID:32893267 PMID:33164571


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623439 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15176425 PMID:19716085 PMID:19862833 PMID:21306642 PMID:22581653 PMID:22685113 PMID:24144883 PMID:24631775 PMID:25175087 PMID:25741868 PMID:26214305 PMID:26467025 PMID:27650965 PMID:28492532 PMID:29247119 PMID:29396561 PMID:33338828 PMID:34426522


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623584 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11710892 PMID:19597050 PMID:20129283 PMID:22581653 PMID:24033266 PMID:24400668 PMID:24613995 PMID:24681144 PMID:25741868 PMID:26743238 PMID:28492532 PMID:29728395 PMID:29970176


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598301 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10940383 PMID:11827685 PMID:14961552 PMID:15266024 PMID:17141278 PMID:19026623 PMID:22247482 PMID:22581653 PMID:23139254 PMID:24190697 PMID:25326637 PMID:25741868 PMID:26798387 PMID:28152038 PMID:28492532 PMID:30609406 PMID:32553838 PMID:33221895 PMID:34649698


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623523 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:15996170 PMID:16414944 PMID:16453024 PMID:19841300 PMID:20129283 PMID:21321465 PMID:22378279 PMID:22490985 PMID:22581653 PMID:23465283 PMID:23692053 PMID:24033266 PMID:24055113 PMID:25637381 PMID:25741868 PMID:28341781 PMID:28492532 PMID:33131149 PMID:33232181 PMID:34219138 PMID:37461109


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:155966988 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:29892087 PMID:32893267


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623547 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19862833 PMID:22581653 PMID:25741868 PMID:25904541 PMID:28492532 PMID:30079003 PMID:32470535 PMID:32893267 PMID:34486814


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623452 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851228 PMID:16344400 PMID:18378609 PMID:20129283 PMID:21109022 PMID:21840964 PMID:22581653 PMID:23671135 PMID:24295898 PMID:25194972 PMID:25741868 PMID:26713557 PMID:27930701 PMID:28341781 PMID:28492532 PMID:29709101 PMID:32893267


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623818 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:17905336 PMID:20137763 PMID:21908450 PMID:22581653 PMID:25741868 PMID:25904541 PMID:27930701 PMID:28412158 PMID:28492532 PMID:30828412 PMID:32746448 PMID:32893267 PMID:35113648


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623504 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11997281 PMID:14760488 PMID:15840476 PMID:18071069 PMID:19716085 PMID:19841300 PMID:20129283 PMID:20486126 PMID:22378279 PMID:22581653 PMID:23414114 PMID:23631430 PMID:23861362 PMID:24033266 PMID:24055113 PMID:24613995 PMID:24713084 PMID:25637381 PMID:25650408 PMID:25741868 PMID:26669661 PMID:27153395 PMID:27435932 PMID:27930701 PMID:28412158 PMID:28492532 PMID:28798025 PMID:29728395 PMID:29874177 PMID:30079003 PMID:30193851 PMID:31262209 PMID:31737537 PMID:32516855 PMID:32553227 PMID:34461752


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623695 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:20129283 PMID:22581653 PMID:24033266 PMID:24136861 PMID:25351510 PMID:25741868 PMID:25904541 PMID:27566755 PMID:28492532 PMID:34935411


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623506 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12673799 PMID:14998624 PMID:20129283 PMID:22378279 PMID:22581653 PMID:23414114 PMID:25741868 PMID:28492532 PMID:30193851


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602114 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15996170 PMID:18378609 PMID:19026623 PMID:22581653 PMID:23631430 PMID:24055113 PMID:24784157 PMID:25410959 PMID:25637381 PMID:25741868 PMID:25904541 PMID:28341781 PMID:28492532 PMID:29449639 PMID:30193851 PMID:32917565 PMID:33919104 PMID:34019817 PMID:37432518


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623648 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:10508990 PMID:10961955 PMID:10973849 PMID:17210839 PMID:17210841 PMID:17646591 PMID:18451998 PMID:19716085 PMID:19841300 PMID:22378279 PMID:22581653 PMID:22685113 PMID:23465283 PMID:24033266 PMID:24055113 PMID:24144883 PMID:24613995 PMID:24631775 PMID:25210526 PMID:25351510 PMID:25410959 PMID:25637381 PMID:25741868 PMID:25904541 PMID:26743238 PMID:26746457 PMID:26822237 PMID:28341588 PMID:28412158 PMID:28492532 PMID:28988457 PMID:29247119 PMID:29331327 PMID:29764897 PMID:29790872 PMID:30847666 PMID:31019283 PMID:31043699 PMID:32048431 PMID:32652122 PMID:34426522 PMID:36129056


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057250 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:30279931 PMID:32533946


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598316 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15338453 PMID:20129283 PMID:22581653 PMID:25741868 PMID:27554632 PMID:28492532 PMID:30193851 PMID:32533946


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10042289 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16199547 PMID:20129283 PMID:22090165 PMID:22090166 PMID:22789973 PMID:25741868 PMID:28492532 PMID:33029862 PMID:36007526


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623822 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:16414944 PMID:21126620 PMID:22581653 PMID:25741868 PMID:28087622 PMID:28492532 PMID:29132927 PMID:31865383 PMID:36303204


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598288 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:1097384 PMID:10973849 PMID:15051636 PMID:15840476 PMID:16344400 PMID:19026623 PMID:19841300 PMID:21185501 PMID:22581653 PMID:25294783 PMID:25741868 PMID:26803770 PMID:27566755 PMID:28492532 PMID:29691127 PMID:30369311 PMID:31057083 PMID:31983221 PMID:32383558 PMID:32893267 PMID:32931730 PMID:35052356 PMID:7889574 PMID:8541846 PMID:8620612 PMID:8917568


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:9692163 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:25904541 PMID:28492532 PMID:29033053 PMID:31737537 PMID:35703482


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:12839816 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:17576681 PMID:19251209 PMID:21321465 PMID:25741868 PMID:28492532 PMID:29709244 PMID:33221895 PMID:35124229 PMID:36197721 PMID:36578016 PMID:9536098


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057295 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:23321620 PMID:24190697 PMID:25741868 PMID:28341781 PMID:28492532 PMID:31696929 PMID:32893267


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623752 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:14523039 PMID:18809926 PMID:2030070 PMID:20384651 PMID:20539757 PMID:22581653 PMID:24948852 PMID:25741868 PMID:26031372 PMID:27082542 PMID:28492532 PMID:28781330 PMID:29709101 PMID:29728395 PMID:31191357 PMID:31447099 PMID:31928070 PMID:32371921 PMID:32533946 PMID:32850980 PMID:32893267 PMID:34539730 PMID:35027292 PMID:35124229 PMID:37061847


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598306 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11710892 PMID:18378609 PMID:19716085 PMID:22581653 PMID:25741868 PMID:28492532 PMID:29544605


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623793 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:12209021 PMID:12566525 PMID:12650885 PMID:12695286 PMID:17088455 PMID:17905336 PMID:19841300 PMID:21350584 PMID:22370996 PMID:22373669 PMID:22581653 PMID:25348405 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11090592 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25163546 PMID:25741868 PMID:26173111 PMID:27041150 PMID:28069705 PMID:28492532 PMID:30084490 PMID:34755423 PMID:35932045 PMID:36303204


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057182 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19716085 PMID:20129283 PMID:22277643 PMID:22789973 PMID:25741868 PMID:26173111 PMID:26467377 PMID:27232914 PMID:27287068 PMID:28492532 PMID:30193851 PMID:31447099 PMID:32048431 PMID:32893267 PMID:34546463


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623534 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18304999 PMID:20129283 PMID:22581653 PMID:22956155 PMID:25741868 PMID:25904541 PMID:28492532 PMID:30193851 PMID:32268277 PMID:32533946 PMID:32893267 PMID:461398


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13542076 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:1309946 PMID:17210841 PMID:25741868 PMID:25904541 PMID:26746457 PMID:28087566 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057227 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:26746457 PMID:28492532 PMID:29517769 PMID:30847666 PMID:31737537 PMID:36973604


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623592 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15851227 PMID:19841300 PMID:20129283 PMID:22581653 PMID:25741868 PMID:25904541 PMID:28492532 PMID:33641026


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623747 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18752142 PMID:19716085 PMID:22581653 PMID:22685113 PMID:24144883 PMID:25741868 PMID:25904541 PMID:26159999 PMID:28492532 PMID:30609406 PMID:31447099 PMID:31928070 PMID:31983221 PMID:35535697


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8602112 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:18378609 PMID:19808477 PMID:22581653 PMID:25650408 PMID:25741868 PMID:28086167 PMID:28150151 PMID:28492532 PMID:29709244 PMID:30086531 PMID:30193851 PMID:32826072 PMID:32893267


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623524 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15176425 PMID:20566482 PMID:22581653 PMID:25741868 PMID:28492532 PMID:29748316 PMID:34379075


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8598317 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:11901046 PMID:15178757 PMID:15579534 PMID:18180363 PMID:18378609 PMID:19026623 PMID:19716085 PMID:20129283 PMID:20403459 PMID:22581653 PMID:23321620 PMID:24573164 PMID:25741868 PMID:28391114 PMID:28492532 PMID:29579189 PMID:30847666 PMID:31019283 PMID:32893267 PMID:34426522


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens) & RGD:11582690|RGD:11583636|RGD:11583679|RGD:11583720|RGD:11584776|RGD:11584982|RGD:11585200|RGD:11585282|RGD:11585310|RGD:11585502|RGD:11585508|RGD:11585916|RGD:11585958|RGD:11586592|RGD:11586627|RGD:11586839|RGD:11587069|RGD:11587755|RGD:11587976|RGD:11588078|RGD:11644615|RGD:11644925|RGD:11645563|RGD:11646462|RGD:11646848|RGD:11648203|RGD:11648243|RGD:11650684|RGD:11651804|RGD:11653262|RGD:11653568|RGD:25314785|RGD:28869786|RGD:28869999|RGD:28870245|RGD:28870251|RGD:28870266|RGD:28870671|RGD:28871766|RGD:28872038|RGD:28872043|RGD:28872329|RGD:28872597|RGD:28872600|RGD:28872609|RGD:28872626|RGD:28873620|RGD:28876419|RGD:28876429|RGD:28876748|RGD:28878759|RGD:28879158|RGD:28879171|RGD:28879552|RGD:28880287|RGD:28881260|RGD:28884000|RGD:28884814|RGD:28885141|RGD:28885153|RGD:28903836|RGD:28903848|RGD:28904658|RGD:28905135|RGD:40814327 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens) & RGD:8603041|RGD:8611142|RGD:8611158|RGD:8611159|RGD:8611166|RGD:8611169|RGD:8611180|RGD:8692780 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:10057235|RGD:12881866|RGD:12891775 (Homo sapiens) & RGD:10057235|RGD:12881866|RGD:12891775 (Homo sapiens) & RGD:10057235|RGD:12881866|RGD:12891775 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:25904541 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:13817203|RGD:34891467 (Homo sapiens) & RGD:13817203|RGD:34891467 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:25741868 PMID:28492532 PMID:31983221


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens) & RGD:11092458|RGD:8611144|RGD:8611173|RGD:8692779|RGD:8692783|RGD:9688080|RGD:9688081|RGD:9690481|RGD:9690917 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:11525758|RGD:12892747|RGD:13810191|RGD:28875583|RGD:28883405 (Homo sapiens) & RGD:11525758|RGD:12892747|RGD:13810191|RGD:28875583|RGD:28883405 (Homo sapiens) & RGD:11525758|RGD:12892747|RGD:13810191|RGD:28875583|RGD:28883405 (Homo sapiens) & RGD:11525758|RGD:12892747|RGD:13810191|RGD:28875583|RGD:28883405 (Homo sapiens) & RGD:11525758|RGD:12892747|RGD:13810191|RGD:28875583|RGD:28883405 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623738 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19862833 PMID:22581653 PMID:25741868 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8603039|RGD:8603043|RGD:9689344 (Homo sapiens) & RGD:8603039|RGD:8603043|RGD:9689344 (Homo sapiens) & RGD:8603039|RGD:8603043|RGD:9689344 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:28884018 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:28492532 PMID:29192238


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8623473 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:15840476 PMID:19841300 PMID:22378279 PMID:22581653 PMID:24721456 PMID:25741868 PMID:28492532 PMID:31737537 PMID:37904629


    • An association has been curated linking SCN5A and long QT syndrome 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred by association of genotype and phenotype with RGD:8611146|RGD:8611157 (Homo sapiens) & RGD:8611146|RGD:8611157 (Homo sapiens)
  • 2 RGD objects have been annotated to long QT syndrome 3  (DOID:0110646)
  • 15 papers in RGD have been used to annotate SCN5A
  • Curation Notes: ClinVar Annotator: match by term: Long QT syndrome 3
  • Original References(s): PMID:19841300 PMID:20129283 PMID:22581653 PMID:24033266 PMID:25741868 PMID:28492532


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