Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR Next-generation sequencing for the diagnosis of hereditary breast and ovarian cancer using genomic capture targeting multiple candidate genes. 24549055

2014

dbSNP: rs80358711
rs80358711
G 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: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations among ovarian cancer patients from Colombia. 22044689

2012

dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR BRCA1, BRCA2, TP53, and CDKN2A germline mutations in patients with breast cancer and cutaneous melanoma. 17624602

2007

dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years. 16912212

2006

dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR Prevalence of BRCA1 and BRCA2 mutations in women diagnosed with ductal carcinoma in situ. 15728167

2005

dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR Cancer variation associated with the position of the mutation in the BRCA2 gene. 15131399

2004

dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR Individual and family characteristics associated with protein truncating BRCA1 and BRCA2 mutations in an Ontario population based series from the Cooperative Family Registry for Breast Cancer Studies. 12920083

2003

dbSNP: rs80358711
rs80358711
G 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in central and southern Italian patients. 11056688

2000

dbSNP: rs80358711
rs80358711
A 0.700 CausalMutation CLINVAR