Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878854131
rs878854131
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome
G 0.700 GeneticVariation CLINVAR Werner syndrome and mutations of the WRN and LMNA genes in France. 16786514

2006

dbSNP: rs878854131
rs878854131
WRN
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome
G 0.700 CausalMutation CLINVAR Werner syndrome and mutations of the WRN and LMNA genes in France. 16786514

2006