Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1383589957
rs1383589957
WRN
G 0.700 CausalMutation CLINVAR A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay. 15888165

2005

dbSNP: rs113993961
rs113993961
WRN
C 0.700 CausalMutation CLINVAR Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products. 10543396

1999

dbSNP: rs113993961
rs113993961
WRN
C 0.700 CausalMutation CLINVAR Prevalence of Werner's syndrome heterozygotes in Japan. 10347997

1999

dbSNP: rs113993961
rs113993961
WRN
C 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

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: rs17847577
rs17847577
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

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

dbSNP: rs113993961
rs113993961
WRN
C 0.700 CausalMutation CLINVAR Positional cloning of the Werner's syndrome gene. 8602509

1996

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

1996

dbSNP: rs17847577
rs17847577
WRN
T 0.700 CausalMutation CLINVAR Homozygous and compound heterozygous mutations at the Werner syndrome locus. 8968742

1996

dbSNP: rs1198210848
rs1198210848
WRN
T 0.700 CausalMutation CLINVAR

dbSNP: rs121908447
rs121908447
WRN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1244318419
rs1244318419
WRN
G 0.700 CausalMutation CLINVAR

dbSNP: rs1284409960
rs1284409960
WRN
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1303126572
rs1303126572
WRN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1361270203
rs1361270203
WRN
CCT 0.700 CausalMutation CLINVAR

dbSNP: rs1554519254
rs1554519254
WRN
GAA 0.700 CausalMutation CLINVAR

dbSNP: rs1554526707
rs1554526707
WRN
TA 0.700 CausalMutation CLINVAR

dbSNP: rs1554527775
rs1554527775
WRN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554528411
rs1554528411
WRN
A 0.700 CausalMutation CLINVAR

dbSNP: rs1563331288
rs1563331288
WRN
G 0.700 CausalMutation CLINVAR

dbSNP: rs1563338837
rs1563338837
WRN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563338855
rs1563338855
WRN
C 0.700 CausalMutation CLINVAR

dbSNP: rs1563357741
rs1563357741
WRN
T 0.700 CausalMutation CLINVAR

dbSNP: rs1563376347
rs1563376347
WRN
A 0.700 CausalMutation CLINVAR