Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Multiple-gene panel analysis in a case series of 255 women with hereditary breast and ovarian cancer. 28423363

2017
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients. 28724667

2017
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Screening for BRCA1 and BRCA2 mutations among French-Canadian breast cancer cases attending an outpatient clinic in Montreal. 23621881

2014
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Genomic aberrations of BRCA1-mutated fallopian tube carcinomas. 24726640

2014
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Contribution of germline mutations in the BRCA and PALB2 genes to pancreatic cancer in Italy. 21989927

2012
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Characteristics and spectrum of BRCA1 and BRCA2 mutations in 3,922 Korean patients with breast and ovarian cancer. 22798144

2012
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Identification of BRCA1-deficient ovarian cancers. 21371001

2011
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer. 21324516

2011
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Non-founder BRCA1 mutations in Russian breast cancer patients. 20727672

2010
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1/2 in high-risk African American women with breast cancer: providing genetic testing through various recruitment strategies. 18752448

2008
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area. 16168118

2005
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR [Analysis of the mutations of BRCA1 in 9 familiar breast cancer patients]. 12947551

2003
dbSNP: rs80357868
rs80357868
BRCA1
T 0.700 CausalMutation CLINVAR Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer. 7894491

1994