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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV496426 and Ventricular Septal Defect 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
  • 1 RGD objects have been annotated to Ventricular Septal Defect 3  (DOID:9003006)
  • 0 papers in RGD have been used to annotate CV496426
  • Curation Notes: ClinVar Annotator: match by term: Ventricular septal defect 3
  • Original References(s): PMID:12798584 PMID:14607454 PMID:24033266 PMID:25741868 PMID:28492532


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