RGD Annotation Report for Congenital Aural AtresiaRat Genome Database

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An association has been curated linking LOC130062726 and Congenital Aural Atresia 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
The annotation has been inferred by association of genotype and phenotype with RGD:405291276 (Homo sapiens)
5 RGD objects have been annotated to Congenital Aural Atresia (DOID:9004309)
0 papers in RGD have been used to annotate LOC130062726
Curation Notes: ClinVar Annotator: match by term: Aural atresia, congenital

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