RGD Annotation Report for Fanconi anemia complementation group GRat Genome Database

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An association has been curated linking CV917998 and Fanconi anemia complementation group G 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 Fanconi anemia complementation group G (DOID:0111086)
0 papers in RGD have been used to annotate CV917998
Curation Notes: ClinVar Annotator: match by term: Fanconi anemia, complementation group G

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