RGD Annotation Report for genetic diseaseRat Genome Database

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An association has been curated linking OSBPL7 and genetic disease 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:155969781 (Homo sapiens)
23840 RGD objects have been annotated to genetic disease (DOID:630)
3 papers in RGD have been used to annotate OSBPL7
Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases

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