RGD Annotation Report for Werner syndromeRat Genome Database

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An association has been curated linking CV523453 and Werner 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
7 RGD objects have been annotated to Werner syndrome (DOID:5688)
0 papers in RGD have been used to annotate CV523453
Curation Notes: ClinVar Annotator: match by term: Werner 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.