Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13266634
rs13266634
T 1.000 SusceptibilityMutation CLINVAR

dbSNP: rs4402960
rs4402960
T 1.000 SusceptibilityMutation CLINVAR

dbSNP: rs12255372
rs12255372
T 0.900 SusceptibilityMutation CLINVAR

dbSNP: rs114202595
rs114202595
A 0.850 CausalMutation CLINVAR

dbSNP: rs121918673
rs121918673
C 0.810 CausalMutation CLINVAR

dbSNP: rs104893649
rs104893649
A 0.800 CausalMutation CLINVAR

dbSNP: rs11196205
rs11196205
C 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs119489103
rs119489103
A 0.800 CausalMutation CLINVAR

dbSNP: rs121434593
rs121434593
T 0.800 CausalMutation CLINVAR

dbSNP: rs121913150
rs121913150
T 0.800 CausalMutation CLINVAR

dbSNP: rs137853240
rs137853240
A 0.800 SusceptibilityMutation CLINVAR

dbSNP: rs3792267
rs3792267
A 0.770 SusceptibilityMutation CLINVAR

dbSNP: rs137852783
rs137852783
A 0.760 SusceptibilityMutation CLINVAR

dbSNP: rs2975760
rs2975760
C 0.730 SusceptibilityMutation CLINVAR

dbSNP: rs5030952
rs5030952
T 0.730 SusceptibilityMutation CLINVAR

dbSNP: rs137852786
rs137852786
A 0.720 SusceptibilityMutation CLINVAR

dbSNP: rs3842570
rs3842570
AGATGATTCTGTCCCAGGAGCCGGGAGGAGGGT 0.720 SusceptibilityMutation CLINVAR

dbSNP: rs104893642
rs104893642
C 0.710 CausalMutation CLINVAR

dbSNP: rs137852785
rs137852785
C 0.710 SusceptibilityMutation CLINVAR

dbSNP: rs200998587
rs200998587
T 0.710 SusceptibilityMutation CLINVAR

dbSNP: rs2070895
rs2070895
A 0.710 SusceptibilityMutation CLINVAR

dbSNP: rs121918407
rs121918407
C 0.700 CausalMutation CLINVAR

dbSNP: rs1259467443
rs1259467443
T 0.700 CausalMutation CLINVAR

dbSNP: rs1339616347
rs1339616347
WRN
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1360415315
rs1360415315
T 0.700 CausalMutation CLINVAR