RGD Annotation Report for Atrioventricular Septal Defect 2Rat Genome Database

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An association has been curated linking CV519647 and Atrioventricular Septal Defect 2 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
40 RGD objects have been annotated to Atrioventricular Septal Defect 2 (DOID:9009051)
0 papers in RGD have been used to annotate CV519647
Curation Notes: ClinVar Annotator: match by term: Atrioventricular septal defect 2
Original References(s): PMID:28492532

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.