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VARIANT - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CV39058 and Ventricular Septal Defect 1 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • 5 RGD objects have been annotated to Ventricular Septal Defect 1  (DOID:9003959)
  • 1 papers in RGD have been used to annotate CV39058
  • Curation Notes: ClinVar Annotator: match by term: Ventricular septal defect 1
  • Original References(s): PMID:18672102 PMID:19302747 PMID:19678963 PMID:21110066 PMID:21519287 PMID:24033266 PMID:25741868 PMID:26490186 PMID:26997702 PMID:28492532 PMID:32992319


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