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An association has been curated linking CV2767177 and genetic 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
27242 RGD objects have been annotated to genetic disease (DOID:630)
0 papers in RGD have been used to annotate CV2767177
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases

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