Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE. 23628597

2013

dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO). 22762150

2012

dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011

dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Risk of breast cancer in male BRCA2 carriers. 20587410

2010

dbSNP: rs80359636
rs80359636
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: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Prevalence and characteristics of pancreatic cancer in families with BRCA1 and BRCA2 mutations. 18855126

2009

dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Associations of high-grade prostate cancer with BRCA1 and BRCA2 founder mutations. 19188187

2009

dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Breast cancer risk among male BRCA1 and BRCA2 mutation carriers. 18042939

2007

dbSNP: rs80359636
rs80359636
T 0.700 CausalMutation CLINVAR Cancer risks in BRCA2 families: estimates for sites other than breast and ovary. 16141007

2005