Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057517565
rs1057517565
T 0.700 GeneticVariation CLINVAR Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries. 26187060

2016

dbSNP: rs1057517566
rs1057517566
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517572
rs1057517572
AT 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517595
rs1057517595
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517636
rs1057517636
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057517865
rs1057517865
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518635
rs1057518635
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518637
rs1057518637
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518638
rs1057518638
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519559
rs1057519559
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057520636
rs1057520636
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499566
rs1060499566
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060499833
rs1060499833
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060502385
rs1060502385
TT 0.700 CausalMutation CLINVAR

dbSNP: rs1060502391
rs1060502391
C 0.700 CausalMutation CLINVAR

dbSNP: rs1060502392
rs1060502392
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502395
rs1060502395
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502400
rs1060502400
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502403
rs1060502403
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502414
rs1060502414
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502426
rs1060502426
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502433
rs1060502433
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502437
rs1060502437
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502444
rs1060502444
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060502449
rs1060502449
T 0.700 CausalMutation CLINVAR