rs1346044, WRN

N. diseases: 23
Disease: Werner Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Werner Syndrome
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