Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ. 22009639

2012
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Spectrum of BRCA1/2 point mutations and genomic rearrangements in high-risk breast/ovarian cancer Chilean families. 20859677

2011
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs11571658
rs11571658
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: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. 23199084

2010
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Prostate cancer in BRCA2 germline mutation carriers is associated with poorer prognosis. 20736950

2010
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in a South American population. 16616110

2006
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects. 12955716

2003
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR A breast cancer family from Spain with germline mutations in both the BRCA1 and BRCA2 genes. 12161611

2002
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Mutation analysis of the BRCA1 and BRCA2 genes results in the identification of novel and recurrent mutations in 6/16 flemish families with breast and/or ovarian cancer but not in 12 sporadic patients with early-onset disease. Mutations in brief no. 224. Online. 10090482

1999
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR High frequency of BRCA1/2 germline mutations in 42 Belgian families with a small number of symptomatic subjects. 10227398

1999
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR BRCA2 germ-line mutations are frequent in male breast cancer patients without a family history of the disease. 9537231

1998
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Evidence of founder mutations in Finnish BRCA1 and BRCA2 families. 9585608

1998
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR A polymorphic stop codon in BRCA2. 8896551

1996
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Identification of the breast cancer susceptibility gene BRCA2. 8524414

1996