Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer. 22798144

2012

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR BRCA1/BRCA2 mutation status and clinical-pathologic features of 108 male breast cancer cases from Tuscany: a population-based study in central Italy. 18819001

2009

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR Founder mutations account for the majority of BRCA1-attributable hereditary breast/ovarian cancer cases in a population from Tuscany, Central Italy. 18821011

2009

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR Genetic epidemiology of BRCA mutations--family history detects less than 50% of the mutation carriers. 17574839

2007

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR Founder mutations in BRCA1 and BRCA2 genes. 17591843

2007

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR BRCA1 mutations in ovarian cancer and borderline tumours in Norway: a nested case-control study. 15477862

2004

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR The Norwegian founder mutations in BRCA1: high penetrance confirmed in an incident cancer series and differences observed in the risk of ovarian cancer. 14522380

2003

dbSNP: rs80357635
rs80357635
C 0.700 GeneticVariation CLINVAR Characterization of ten novel and 13 recurring BRCA1 and BRCA2 germline mutations in Italian breast and/or ovarian carcinoma patients. Mutations in brief no. 178. Online. 10660329

1998

dbSNP: rs80357635
rs80357635
C 0.700 CausalMutation CLINVAR