Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes. 25085752

2014

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Founder BRCA1/2 mutations in the Europe: implications for hereditary breast-ovarian cancer prevention and control. 23199084

2010

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR A role of BRCA1 and BRCA2 germline mutations in breast cancer susceptibility within Sardinian population. 19619314

2009

dbSNP: rs80359714
rs80359714
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: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Founder mutations in BRCA1 and BRCA2 genes. 17591843

2007

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Spectrum and prevalence of BRCA1 and BRCA2 germline mutations in Sardinian patients with breast carcinoma through hospital-based screening. 16047344

2005

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR The 8765delAG mutation in BRCA2 is common among Jews of Yemenite extraction. 9634522

1998

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Founder BRCA1 and BRCA2 mutations in French Canadian breast and ovarian cancer families. 9792861

1998

dbSNP: rs80359714
rs80359714
A 0.700 CausalMutation CLINVAR Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. 8673090

1996