Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR The role of targeted BRCA1/BRCA2 mutation analysis in hereditary breast/ovarian cancer families of Portuguese ancestry. 24916970

2015

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Central European BRCA2 mutation carriers: birth cohort status correlates with onset of breast cancer. 24156927

2014

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease. 24556621

2014

dbSNP: rs80359212
rs80359212
T 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: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Identification of a novel in-frame deletion in BRCA2 and analysis of variants of BRCA1/2 in Italian patients affected with hereditary breast and ovarian cancer. 23096105

2012

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Expression of cancer testis antigens in human BRCA-associated breast cancers: potential targets for immunoprevention? 21465317

2011

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Prostate cancer in BRCA2 germline mutation carriers is associated with poorer prognosis. 20736950

2010

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study. 20104584

2010

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Breast cancer in young women (YBC): prevalence of BRCA1/2 mutations and risk of secondary malignancies across diverse racial groups. 19491284

2009

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Cross-sectional analysis of germline BRCA1 and BRCA2 mutations in Japanese patients suspected to have hereditary breast/ovarian cancer. 19016756

2008

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer. 18465347

2008

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 genetic testing in Hispanic patients: mutation prevalence and evaluation of the BRCAPRO risk assessment model. 17925560

2007

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer. 16905680

2007

dbSNP: rs80359212
rs80359212
T 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: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR Identification and evaluation of 55 genetic variations in the BRCA1 and the BRCA2 genes of patients from 50 Japanese breast cancer families. 15168169

2004

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR BRCA1/2 mutations in Swiss patients with familial or early-onset breast and ovarian cancer. 11400546

2001

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR BRCA2 germline mutations among early onset breast cancer patients unselected for family history of the disease. 10978364

2000

dbSNP: rs80359212
rs80359212
T 0.700 CausalMutation CLINVAR A standardized technique for the placement of electrodes in the two heads of the lateral pterygoid muscle. 2073695

1990