RGD Annotation Report for Usher syndrome type 2ARat Genome Database

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An association has been curated linking CV84447 and Usher syndrome type 2A 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
11 RGD objects have been annotated to Usher syndrome type 2A (DOID:0110838)
1 papers in RGD have been used to annotate CV84447
Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 2A
Original References(s): PMID:25741868 PMID:26667666 PMID:26806561 PMID:26927203 PMID:28492532 PMID:32531858 PMID:34906470

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