Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Identification of novel BRCA founder mutations in Middle Eastern breast cancer patients using capture and Sanger sequencing analysis. 27082205

2016
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR The prevalence and spectrum of BRCA1 and BRCA2 mutations in Korean population: recent update of the Korean Hereditary Breast Cancer (KOHBRA) study. 25863477

2015
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer. 25452441

2015
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Association of BRCA1 germline mutations in young onset triple-negative breast cancer (TNBC). 23982851

2014
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Evaluation of BRCA1 mutations in an unselected patient population with triple-negative breast cancer. 23192404

2013
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Predictive factors for BRCA1/BRCA2 mutations in women with ductal carcinoma in situ. 22009639

2012
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Germline mutations in BRCA1 and BRCA2 genes in ethnically diverse high risk families in Israel. 20960228

2011
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311

2011
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes. 21702907

2011
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Application of embryonic lethal or other obvious phenotypes to characterize the clinical significance of genetic variants found in trans with known deleterious mutations. 16267036

2005
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR A low frequency of non-founder BRCA1 mutations in Ashkenazi Jewish breast-ovarian cancer families. 12402332

2002
dbSNP: rs80356885
rs80356885
BRCA1
T 0.700 CausalMutation CLINVAR Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer. 11504767

2001