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 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 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 Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

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
CA 0.700 CausalMutation CLINVAR Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. 23199084

2010
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR Founder mutations among the Dutch. 15010701

2004
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer families. 11597388

2001
dbSNP: rs80359507
rs80359507
BRCA2
CA 0.700 CausalMutation CLINVAR Screening for BRCA2 mutations in 81 Dutch breast-ovarian cancer families. 10638982

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

1997
dbSNP: rs80359507
rs80359507
BRCA2
C 0.700 CausalMutation CLINVAR BRCA2 mutations in hereditary breast and ovarian cancer in France. 9150172

1997
dbSNP: rs80359507
rs80359507
BRCA2
CAA 0.700 CausalMutation CLINVAR