Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs776785728
rs776785728
WRN
T 0.700 CausalMutation CLINVAR The clinical characteristics of Werner syndrome: molecular and biochemical diagnosis. 18810497

2008
dbSNP: rs776785728
rs776785728
WRN
T 0.700 CausalMutation CLINVAR Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population. 9225981

1997