Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Increased risk of male cancer and identification of a potential prostate cancer cluster region in BRCA2. 26360800

2016
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer. 25682074

2015
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study. 25863477

2015
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study. 25863477

2015
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR The contribution of deleterious germline mutations in BRCA1, BRCA2 and the mismatch repair genes to ovarian cancer in the population. 24728189

2014
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. 24504028

2014
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Nonequivalent gene expression and copy number alterations in high-grade serous ovarian cancers with BRCA1 and BRCA2 mutations. 23633455

2013
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer. 23569316

2013
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Description and analysis of genetic variants in French hereditary breast and ovarian cancer families recorded in the UMD-BRCA1/BRCA2 databases. 22144684

2012
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families. 22923021

2012
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR The occurrence of germline BRCA1 and BRCA2 sequence alterations in Slovenian population. 21232165

2011
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311

2011
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311

2011
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer. 21233401

2011
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer. 18465347

2008
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR A DGGE system for comprehensive mutation screening of BRCA1 and BRCA2: application in a Dutch cancer clinic setting. 16683254

2006
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR The breast cancer information core: database design, structure, and scope. 10923033

2000
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes. 10486320

1999
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR Survival in hereditary breast cancer associated with germline mutations of BRCA2. 10550133

1999
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. 9585613

1998
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. 8988179

1997