Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908446
rs121908446
WRN
T 0.700 CausalMutation CLINVAR Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group. 9012406

1997
dbSNP: rs121908446
rs121908446
WRN
T 0.700 CausalMutation CLINVAR Positional cloning of the Werner's syndrome gene. 8602509

1996