Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894136
rs104894136
CYP17A1 ; WBP1L ; CYP17A1-AS1
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs112294663
rs112294663
PHB
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs118203998
rs118203998
PALB2
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs118203999
rs118203999
PALB2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs121908698
rs121908698
CHEK2
T 0.700 CausalMutation CLINVAR

dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs137853011
rs137853011
CHEK2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555284566
rs1555284566
BRCA2
GT 0.700 GeneticVariation CLINVAR

dbSNP: rs1555287661
rs1555287661
BRCA2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555288169
rs1555288169
BRCA2
CT 0.700 GeneticVariation CLINVAR

dbSNP: rs1555591746
rs1555591746
BRCA1
TA 0.700 GeneticVariation CLINVAR

dbSNP: rs17879961
rs17879961
CHEK2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1801155
rs1801155
APC
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs180177097
rs180177097
PALB2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs180177102
rs180177102
PALB2
C 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs180177111
rs180177111
PALB2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs180177132
rs180177132
PALB2
T 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs180177133
rs180177133
PALB2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs28904921
rs28904921
ATM ; C11orf65
G 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs555607708
rs555607708
CHEK2
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs555607708
rs555607708
CHEK2
A 0.700 CausalMutation CLINVAR

dbSNP: rs587781707
rs587781707
BARD1
C 0.700 CausalMutation CLINVAR

dbSNP: rs587781837
rs587781837
ATM ; C11orf65
C 0.700 CausalMutation CLINVAR

dbSNP: rs587781840
rs587781840
PALB2
C 0.700 CausalMutation CLINVAR

dbSNP: rs786203008
rs786203008
ATM ; C11orf65
A 0.700 CausalMutation CLINVAR