WRN, WRN RecQ like helicase, 7486

N. diseases: 172; N. variants: 89
Disease: Werner Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1304645785
rs1304645785
Entrez Id: 7486
Gene Symbol: WRN
WRN
CUI: C0043119
Disease:
Werner Syndrome 		0.010 GeneticVariation BEFREE In this study, we have characterized the G574R missense mutation, which was recently identified in a WS patient. 23583337 2013