Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Prevalence and Prognostic Role of BRCA1/2 Variants in Unselected Chinese Breast Cancer Patients. 27257965

2016
dbSNP: rs80357973
rs80357973
BRCA1
C 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: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 germline mutations and tumor characteristics in Chinese women with familial or early-onset breast cancer. 18512148

2009
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR The prevalence of BRCA1 and BRCA2 germline mutations in high-risk breast cancer patients of Chinese Han nationality: two recurrent mutations were identified. 17851763

2008
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high risk of carrying mutations. 16455195

2007
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR [5589del8: the recurrent mutation of BRCA1 gene in Chinese breast cancer patients]. 17680524

2007
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR [Mutational analysis of BRCA1 and BRCA2 genes in early-onset breast cancer patients in Shanghai]. 16324400

2005
dbSNP: rs80357973
rs80357973
BRCA1
C 0.700 CausalMutation CLINVAR Incidence of BRCA1 and BRCA2 mutations in young Korean breast cancer patients. 15117986

2004