Gene: BRCA1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060505051
rs1060505051
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131692162
rs1131692162
BRCA1
A 0.700 CausalMutation CLINVAR

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

2016
dbSNP: rs397508983
rs397508983
BRCA1
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs398122630
rs398122630
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs41293465
rs41293465
BRCA1
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs62625308
rs62625308
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356923
rs80356923
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80356978
rs80356978
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357123
rs80357123
BRCA1
A 0.700 CausalMutation CLINVAR

dbSNP: rs80357167
rs80357167
BRCA1
A 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs80357303
rs80357303
BRCA1
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80357310
rs80357310
BRCA1
A 0.700 CausalMutation CLINVAR

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

2016
dbSNP: rs80357787
rs80357787
BRCA1
A 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs886037785
rs886037785
BRCA1
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80357714
rs80357714
BRCA1
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1057517590
rs1057517590
BRCA1
C 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs1555599208
rs1555599208
BRCA1
C 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs28897672
rs28897672
BRCA1
C 0.700 CausalMutation CLINVAR

dbSNP: rs397508940
rs397508940
BRCA1
C 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs587781632
rs587781632
BRCA1
C 0.700 GeneticVariation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80357006
rs80357006
BRCA1
C 0.700 CausalMutation CLINVAR

dbSNP: rs80357243
rs80357243
BRCA1
C 0.700 GeneticVariation CLINVAR Comprehensive analysis of missense variations in the BRCT domain of BRCA1 by structural and functional assays. 20516115

2010
dbSNP: rs80357243
rs80357243
BRCA1
C 0.700 GeneticVariation CLINVAR Does familial breast cancer and thymoma suggest a cancer syndrome? A family perspective. 26344711

2015