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GENE - TERM ANNOTATION REPORT

88 Annotations Found.

An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11630233 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:151728434 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:22678886 PMID:25741868 PMID:31773638 PMID:32727330 PMID:36099689


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11629665 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8659301 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:28895250 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8659303 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11647479 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:40905336 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11664146 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11628402 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11635589 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11547612 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11631671 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11625773 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11631251 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:329955103 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:12356851 PMID:25741868


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8600965 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:8755487


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:14693591 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8659304 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:18414213 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11627670 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital Myasthenic Syndrome, Dominant/Recessive
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11627999 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:14717836 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15128110 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15145043 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13489607 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15129850 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:14714960 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11544305 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15140516 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:41407511 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15131754 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:127230836 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13479324 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:26467025


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:12833754 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11552422 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11551816 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8659302 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:12905896 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8600964 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:8755487


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13516319 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8566717 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:14532324 PMID:22678886 PMID:25741868 PMID:28492532 PMID:9158150


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38491969 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38492782 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:127269819 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:22678886 PMID:25741868 PMID:26284228 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126735840 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13465690 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:8604446 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:12141316 PMID:19153382 PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126748795 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126765580 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:8755487


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:14739936 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:28908360 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13611181 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:12742662 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:22382357 PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:12913202 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:21150643 PMID:22678886 PMID:25741868 PMID:27717316 PMID:28492532 PMID:9158150


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11522996 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, slow-channel congenital
  • Original References(s): PMID:20301347 PMID:20562457 PMID:22678886 PMID:24033266 PMID:25741868 PMID:28492532 PMID:29054425 PMID:29383513 PMID:9708546


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15179249 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38498901 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:14739397 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126759303 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126737778 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:127271851 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:20157724 PMID:22678886 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38497242 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13815770 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:26899781 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38490991 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:127331198 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126774956 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38491197 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:126916584 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15040325 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:9539130


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13485354 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38477147 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:15167380 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13475399 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:26923768 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:12898571 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13802989 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11642216 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:12417530 PMID:17878953 PMID:19544078 PMID:21940170 PMID:24033266 PMID:24295813 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29189923 PMID:31980526


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13811196 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38499702 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13611163 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13817897 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:28908356 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:28492532 PMID:9158150


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:38487499 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11522843 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:10496269 PMID:10514102 PMID:10534268 PMID:15322984 PMID:15367858 PMID:25326635 PMID:25741868 PMID:26467025 PMID:27634344 PMID:28492532 PMID:9097970 PMID:9668239


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:26896493 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:12536367 PMID:16199547 PMID:22678886 PMID:25741868 PMID:28464723 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:13611155 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking C17orf107 and congenital myasthenic syndrome 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:11615872 (Homo sapiens)
  • 264 RGD objects have been annotated to congenital myasthenic syndrome  (DOID:3635)
  • 1 papers in RGD have been used to annotate C17orf107
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome
  • Original References(s): PMID:25741868 PMID:28492532


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