Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1085307902
rs1085307902
A 0.700 CausalMutation CLINVAR

dbSNP: rs111312760
rs111312760
A 0.700 CausalMutation CLINVAR

dbSNP: rs1135401857
rs1135401857
A 0.700 CausalMutation CLINVAR

dbSNP: rs1432504119
rs1432504119
A 0.700 CausalMutation CLINVAR

dbSNP: rs1484076591
rs1484076591
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555579633
rs1555579633
A 0.700 CausalMutation CLINVAR Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries. 26187060

2016

dbSNP: rs1555581017
rs1555581017
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555587497
rs1555587497
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555587992
rs1555587992
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555588220
rs1555588220
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555588625
rs1555588625
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555589569
rs1555589569
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555590315
rs1555590315
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555591383
rs1555591383
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555593298
rs1555593298
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555593310
rs1555593310
A 0.700 CausalMutation CLINVAR

dbSNP: rs1567779686
rs1567779686
A 0.700 CausalMutation CLINVAR

dbSNP: rs1567796819
rs1567796819
A 0.700 CausalMutation CLINVAR

dbSNP: rs1567797748
rs1567797748
A 0.700 CausalMutation CLINVAR

dbSNP: rs200432771
rs200432771
A 0.700 CausalMutation CLINVAR Identification of BRCA1/2 founder mutations in Southern Chinese breast cancer patients using gene sequencing and high resolution DNA melting analysis. 22970155

2012

dbSNP: rs273898674
rs273898674
A 0.700 CausalMutation CLINVAR Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries. 26187060

2016

dbSNP: rs273898674
rs273898674
A 0.700 CausalMutation CLINVAR A new BRCA1 mutation in a Filipino woman with a family history of breast and ovarian cancer. 9836072

1998

dbSNP: rs273898674
rs273898674
A 0.700 CausalMutation CLINVAR Evaluation of germline BRCA1 and BRCA2 mutations in a multi-ethnic Asian cohort of ovarian cancer patients. 26541979

2016

dbSNP: rs273898674
rs273898674
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016

dbSNP: rs273899698
rs273899698
A 0.700 CausalMutation CLINVAR