RGD Annotation Report for spinocerebellar ataxia type 13Rat Genome Database

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An association has been curated linking CV442241 and spinocerebellar ataxia type 13 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
2 RGD objects have been annotated to spinocerebellar ataxia type 13 (DOID:0050963)
0 papers in RGD have been used to annotate CV442241
Curation Notes: ClinVar Annotator: match by term: Spinocerebellar ataxia type 13
Original References(s): PMID:25741868 PMID:26467025 PMID:28492532

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