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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV181222 and Coronary Disease in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • 660 RGD objects have been annotated to Coronary Disease  (DOID:9000528)
  • 0 papers in RGD have been used to annotate CV181222
  • Curation Notes: ClinVar Annotator: match by term: Early-onset coronary artery disease
  • Original References(s): PMID:10422804 PMID:11810272 PMID:11845603 PMID:17765246 PMID:19318025 PMID:20506408 PMID:21382890 PMID:21642693 PMID:22390909 PMID:23375686 PMID:24033266 PMID:25487149 PMID:25647241 PMID:25741868 PMID:28161202 PMID:28492532 PMID:28895539 PMID:29353225 PMID:30293936 PMID:30637778 PMID:30971288 PMID:32719484 PMID:33418990 PMID:33454241 PMID:33740630 PMID:34037665 PMID:35339733 PMID:35568682 PMID:36499307 PMID:9712531


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