Gene: BRCA2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11571833
rs11571833
BRCA2
0.720 GeneticVariation BEFREE However, a stop-gain mutation, K3326* (rs11571833), confers risk of lung cancer and cancers of the upper-aero-digestive tract but only a modest risk of breast or ovarian cancer. 29767749

2018
dbSNP: rs11571833
rs11571833
BRCA2
T 0.720 GeneticVariation GWASCAT Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. 27197191

2016
dbSNP: rs11571833
rs11571833
BRCA2
0.720 GeneticVariation BEFREE The K3326X variant was associated with breast (ORw = 1.28, 95% CI = 1.17 to 1.40, P = 5.9x10(-) (6)) and invasive ovarian cancer</span> (ORw = 1.26, 95% CI = 1.10 to 1.43, P = 3.8x10(-3)). 26586665

2016
dbSNP: rs11571818
rs11571818
BRCA2
C 0.700 GeneticVariation GWASCAT Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. 27197191

2016
dbSNP: rs869320800
rs869320800
BRCA2
A 0.700 CausalMutation CLINVAR Nonsense-mediated mRNA decay: terminating erroneous gene expression. 15145354

2004
dbSNP: rs1555283322
rs1555283322
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs1566215870
rs1566215870
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1566221377
rs1566221377
BRCA2
CT 0.700 CausalMutation CLINVAR

dbSNP: rs1566228017
rs1566228017
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1566231316
rs1566231316
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs1566232230
rs1566232230
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1566233171
rs1566233171
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs1566244975
rs1566244975
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs1566260318
rs1566260318
BRCA2
C 0.700 GeneticVariation CLINVAR

dbSNP: rs276174868
rs276174868
BRCA2
C 0.700 CausalMutation CLINVAR

dbSNP: rs397507419
rs397507419
BRCA2
CA 0.700 CausalMutation CLINVAR

dbSNP: rs397507591
rs397507591
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs397507608
rs397507608
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs41293497
rs41293497
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs587781506
rs587781506
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs786203853
rs786203853
BRCA2
CT 0.700 CausalMutation CLINVAR

dbSNP: rs80358533
rs80358533
BRCA2
T 0.700 CausalMutation CLINVAR

dbSNP: rs80358721
rs80358721
BRCA2
G 0.700 CausalMutation CLINVAR

dbSNP: rs80358785
rs80358785
BRCA2
A 0.700 CausalMutation CLINVAR

dbSNP: rs80358920
rs80358920
BRCA2
T 0.700 CausalMutation CLINVAR