Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28897672
rs28897672
BRCA1
C 0.870 CausalMutation CLINVAR

dbSNP: rs28897696
rs28897696
BRCA1
T 0.810 CausalMutation CLINVAR

dbSNP: rs28897759
rs28897759
BRCA2
T 0.810 GeneticVariation CLINVAR

dbSNP: rs28897759
rs28897759
BRCA2
0.810 GeneticVariation UNIPROT

dbSNP: rs55770810
rs55770810
BRCA1
A 0.810 CausalMutation CLINVAR

dbSNP: rs17879961
rs17879961
CHEK2
G 0.800 CausalMutation CLINVAR

dbSNP: rs41293455
rs41293455
BRCA1
A 0.800 CausalMutation CLINVAR

dbSNP: rs41293511
rs41293511
BRCA2
C 0.800 CausalMutation CLINVAR

dbSNP: rs45580035
rs45580035
BRCA2
T 0.800 CausalMutation CLINVAR

dbSNP: rs80357389
rs80357389
BRCA1
A 0.800 CausalMutation CLINVAR

dbSNP: rs80359014
rs80359014
BRCA2
T 0.800 CausalMutation CLINVAR

dbSNP: rs80359014
rs80359014
BRCA2
0.800 GeneticVariation UNIPROT

dbSNP: rs1213469537
rs1213469537
CAV1
0.780 GeneticVariation UNIPROT

dbSNP: rs28904921
rs28904921
ATM ; C11orf65
G 0.780 CausalMutation CLINVAR

dbSNP: rs121434592
rs121434592
AKT1
0.770 GeneticVariation UNIPROT

dbSNP: rs28934578
rs28934578
TP53
T 0.750 CausalMutation CLINVAR

dbSNP: rs28934576
rs28934576
TP53
T 0.740 CausalMutation CLINVAR

dbSNP: rs121913273
rs121913273
PIK3CA
0.730 GeneticVariation UNIPROT

dbSNP: rs180177132
rs180177132
PALB2
T 0.730 GeneticVariation CLINVAR

dbSNP: rs80359065
rs80359065
BRCA2
0.730 GeneticVariation UNIPROT

dbSNP: rs11540652
rs11540652
TP53
T 0.720 CausalMutation CLINVAR

dbSNP: rs138213197
rs138213197
HOXB13
T 0.720 CausalMutation CLINVAR

dbSNP: rs1801155
rs1801155
APC
A 0.720 SusceptibilityMutation CLINVAR

dbSNP: rs180177143
rs180177143
PALB2
G 0.720 GeneticVariation CLINVAR

dbSNP: rs200595749
rs200595749
ZFYVE26
0.720 GeneticVariation UNIPROT