Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62625308
rs62625308
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356923
rs80356923
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356962
rs80356962
T 0.700 CausalMutation CLINVAR

dbSNP: rs80356978
rs80356978
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357006
rs80357006
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357086
rs80357086
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357123
rs80357123
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357167
rs80357167
A 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004

dbSNP: rs80357287
rs80357287
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357303
rs80357303
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016

dbSNP: rs80357310
rs80357310
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357382
rs80357382
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357481
rs80357481
C 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004

dbSNP: rs80357498
rs80357498
T 0.700 CausalMutation CLINVAR Functional differences among BRCA1 missense mutations in the control of centrosome duplication. 21725363

2012

dbSNP: rs80357522
rs80357522
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357580
rs80357580
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016

dbSNP: rs80357701
rs80357701
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357706
rs80357706
T 0.700 CausalMutation CLINVAR

dbSNP: rs80357714
rs80357714
AT 0.700 CausalMutation CLINVAR

dbSNP: rs80357718
rs80357718
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357724
rs80357724
G 0.700 CausalMutation CLINVAR

dbSNP: rs80357760
rs80357760
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357772
rs80357772
C 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004

dbSNP: rs80357772
rs80357772
C 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016

dbSNP: rs80357783
rs80357783
CT 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016