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 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 Screening for BRCA1 and BRCA2 mutations in Eastern Finnish breast/ovarian cancer families. 17850627

2007
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 BRCA1 and BRCA2 mutations in Scotland and Northern Ireland. 12698193

2003
dbSNP: rs11571658
rs11571658
BRCA2
C 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: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503deITT mutation previously found to recur in different ethnic populations. 11359068

2001
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Cancer risks in BRCA2 mutation carriers. 10433620

1999
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Mutation analysis of the BRCA1 and BRCA2 genes in the Belgian patient population and identification of a Belgian founder mutation BRCA1 IVS5 + 3A > G. 10595255

1999
dbSNP: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. 9585613

1998
dbSNP: rs11571658
rs11571658
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: rs11571658
rs11571658
BRCA2
C 0.700 CausalMutation CLINVAR Identification of the breast cancer susceptibility gene BRCA2. 8524414

1996