Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28904921
rs28904921
ATM ; C11orf65
G 0.700 CausalMutation CLINVAR

dbSNP: rs35766612
rs35766612
TGFBR2
0.700 GeneticVariation UNIPROT

dbSNP: rs397507396
rs397507396
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507644
rs397507644
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507649
rs397507649
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507967
rs397507967
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs397509160
rs397509160
BRCA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs397509173
rs397509173
BRCA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs398122630
rs398122630
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs483353077
rs483353077
BRCA2
AAAA 0.700 CausalMutation CLINVAR

dbSNP: rs587776416
rs587776416
PALB2
C 0.700 CausalMutation CLINVAR

dbSNP: rs587782620
rs587782620
TP53
T 0.700 CausalMutation CLINVAR

dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356923
rs80356923
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356962
rs80356962
BRCA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356978
rs80356978
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357006
rs80357006
BRCA1
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357086
rs80357086
BRCA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357123
rs80357123
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357287
rs80357287
BRCA1 ; NBR2
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357310
rs80357310
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357382
rs80357382
BRCA1
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357522
rs80357522
BRCA1
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357701
rs80357701
BRCA1
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357706
rs80357706
BRCA1
T 0.700 CausalMutation CLINVAR