Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Prevalence of Hispanic BRCA1 and BRCA2 mutations among hereditary breast and ovarian cancer patients from Brazil reveals differences among Latin American populations. 27425403

2016

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Detection of BRCA1 and BRCA2 germline mutations in Japanese population using next-generation sequencing. 25802882

2015

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 mutations in males with familial breast and ovarian cancer syndrome. Results of a Spanish multicenter study. 26026974

2015

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. 21952622

2011

dbSNP: rs80359584
rs80359584
A 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: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer. 18489799

2008

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Prevalence of BRCA1 and BRCA2 mutations in breast cancer patients from Brazil. 17063270

2007

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Population BRCA1 and BRCA2 mutation frequencies and cancer penetrances: a kin-cohort study in Ontario, Canada. 17148771

2006

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. 11179017

2001

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Global sequence diversity of BRCA2: analysis of 71 breast cancer families and 95 control individuals of worldwide populations. 9971877

1999

dbSNP: rs80359584
rs80359584
A 0.700 CausalMutation CLINVAR Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. 8988179

1997