RGD Annotation Report for Usher syndrome type 1CRat Genome Database

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An association has been curated linking CV325686 and Usher syndrome type 1C 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 Usher syndrome type 1C (DOID:0110830)
0 papers in RGD have been used to annotate CV325686
Curation Notes: ClinVar Annotator: match by term: Usher syndrome, type 1C
Original References(s): PMID:28492532

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