Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359335
rs80359335
BRCA2
CA 0.700 CausalMutation CLINVAR Development of primary early-onset colorectal cancers due to biallelic mutations of the FANCD1/BRCA2 gene. 24301060

2014
dbSNP: rs80359335
rs80359335
BRCA2
CA 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: rs80359335
rs80359335
BRCA2
CA 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs80359335
rs80359335
BRCA2
CA 0.700 CausalMutation CLINVAR Comprehensive BRCA1 and BRCA2 mutation analyses and review of French Canadian families with at least three cases of breast cancer. 20694749

2010
dbSNP: rs80359335
rs80359335
BRCA2
CA 0.700 CausalMutation CLINVAR Germline mutations in BRCA2: shared genetic susceptibility to breast cancer, early onset leukemia, and Fanconi anemia. 15070707

2004
dbSNP: rs80359335
rs80359335
BRCA2
CA 0.700 CausalMutation CLINVAR Prevalence of BRCA1 and BRCA2 mutations among clinic-based African American families with breast cancer. 11030417

2000
dbSNP: rs80359335
rs80359335
BRCA2
CA 0.700 CausalMutation CLINVAR Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families. 9792861

1998