RGD Annotation Report for autosomal dominant nonsyndromic deafness 4ARat Genome Database

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An association has been curated linking CV176058 and autosomal dominant nonsyndromic deafness 4A 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
3 RGD objects have been annotated to autosomal dominant nonsyndromic deafness 4A (DOID:0110573)
0 papers in RGD have been used to annotate CV176058
Curation Notes: ClinVar Annotator: match by term: MYH14-related condition
Original References(s): PMID:24033266 PMID:25741868 PMID:28492532

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