RGD Annotation Report for HeterotaxyRat Genome Database

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An association has been curated linking CV281031 and Heterotaxy 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
49 RGD objects have been annotated to Heterotaxy (HP:0030853)
0 papers in RGD have been used to annotate CV281031
Curation Notes: ClinVar Annotator: match by term: Heterotaxia

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