Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Spectrum of genetic variants of BRCA1 and BRCA2 in a German single center study. 28324225

2017
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results. 28008555

2017
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Aggregate penetrance of genomic variants for actionable disorders in European and African Americans. 27831900

2016
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome. 27303907

2016
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR A high frequency of BRCA mutations in young black women with breast cancer residing in Florida. 26287763

2015
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Clinical characteristics of ovarian cancer classified by BRCA1, BRCA2, and RAD51C status. 24504028

2014
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screening. 23397983

2014
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 testing should be offered to individuals with triple-negative breast cancer diagnosed below 50 years. 22333603

2012
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Novel BRCA1 and BRCA2 pathogenic mutations in Slovene hereditary breast and ovarian cancer families. 22923021

2012
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Breast cancer risk among male BRCA1 and BRCA2 mutation carriers. 18042939

2007
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR The breast cancer information core: database design, structure, and scope. 10923033

2000
dbSNP: rs80357867
rs80357867
BRCA1
T 0.700 CausalMutation CLINVAR Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer. 9150171

1997