WRN, WRN RecQ like helicase, 7486

N. diseases: 172; N. variants: 89
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268134
Disease: DNA Repair-Deficiency
DNA Repair-Deficiency
0.300 Biomarker phenotype CTD_human Reduction of Werner Syndrome Protein Enhances G:C → A:T Transition by O6-Methylguanine in Human Cells. 29616805 2018