Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Frequent incidence of BARD1-truncating mutations in germline DNA from triple-negative breast cancer patients. 26010302

2016
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Identification of a founder BRCA1 mutation in the Moroccan population. 26864382

2016
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR BRCA genetic screening in Middle Eastern and North African: mutational spectrum and founder BRCA1 mutation (c.798_799delTT) in North African. 25814778

2015
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Prevalence and type of BRCA mutations in Hispanics undergoing genetic cancer risk assessment in the southwestern United States: a report from the Clinical Cancer Genetics Community Research Network. 23233716

2013
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Mutation screening of the BRCA1 gene in early onset and familial breast/ovarian cancer in Moroccan population. 23289006

2013
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR A comprehensive focus on global spectrum of BRCA1 and BRCA2 mutations in breast cancer. 24312913

2013
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR BRCA1 And BRCA2 analysis of Argentinean breastovarian cancer patients selected for age and family history highlights a role for novel mutations of putative south-American origin. 23961350

2012
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Hereditary breast cancer in Middle Eastern and North African (MENA) populations: identification of novel, recurrent and founder BRCA1 mutations in the Tunisian population. 21603858

2012
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes. 21702907

2011
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 germline mutations screening in Algerian breast/ovarian cancer families. 20683152

2010
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR BRCA1 mutations in Algerian breast cancer patients: high frequency in young, sporadic cases. 18645608

2008
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Prevalence of pathogenic BRCA1 mutation carriers in 5 US racial/ethnic groups. 18159056

2007
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR BRCA1 genetic testing in 106 breast and ovarian cancer families from Southern Italy (Sicily): a mutation analyses. 17221156

2007
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation. 7493024

1995
dbSNP: rs80357724
rs80357724
BRCA1
G 0.700 CausalMutation CLINVAR [Effects of extrusion of peas (Pisum sativum) on the intestinal flow of nitrogen in cows]. 2206311

1990