Gene: BRCA2 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518635
rs1057518635
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057518637
rs1057518637
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057518638
rs1057518638
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1131692035
rs1131692035
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555280073
rs1555280073
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555281594
rs1555281594
BRCA2
TG 0.700 CausalMutation CLINVAR

dbSNP: rs1555282830
rs1555282830
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555283169
rs1555283169
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1555284442
rs1555284442
BRCA2
T 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs276174819
rs276174819
BRCA2
CA 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs397507396
rs397507396
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs397507643
rs397507643
BRCA2
C 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs397507644
rs397507644
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507649
rs397507649
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs397507710
rs397507710
BRCA2
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs397507828
rs397507828
BRCA2
T 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs397507967
rs397507967
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs398122710
rs398122710
BRCA2
A 0.700 GeneticVariation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs483353077
rs483353077
BRCA2
AAAA 0.700 CausalMutation CLINVAR

dbSNP: rs483353111
rs483353111
BRCA2
G 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs587782780
rs587782780
BRCA2
T 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs771203198
rs771203198
BRCA2
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80358427
rs80358427
BRCA2
T 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80358529
rs80358529
BRCA2
T 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80358785
rs80358785
BRCA2
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016