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: rs1346044
rs1346044
Entrez Id: 7486
Gene Symbol: WRN
WRN
CUI: C0043119
Disease:
Werner Syndrome 		0.010 GeneticVariation BEFREE Association of the rs1346044 Polymorphism of the Werner Syndrome Gene RECQL2 with Increased Risk and Premature Onset of Breast Cancer. 26690424 2015