RGD Annotation Report for WAGR syndromeRat Genome Database

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An association has been curated linking CV241134 and WAGR syndrome 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
5 RGD objects have been annotated to WAGR syndrome (DOID:14515)
0 papers in RGD have been used to annotate CV241134
Curation Notes: ClinVar Annotator: match by term: CHROMOSOME 11p13 DELETION SYNDROME
Original References(s): PMID:28492532

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