Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357808
rs80357808
BRCA1
T 0.700 CausalMutation CLINVAR Characterization of mutations in BRCA1/2 and the relationship with clinic-pathological features of breast cancer in a hereditarily high-risk sample of chinese population. 29435039

2018
dbSNP: rs80357808
rs80357808
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: rs80357808
rs80357808
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: rs80357808
rs80357808
BRCA1
T 0.700 CausalMutation CLINVAR Performance of BRCA1/2 mutation prediction models in Asian Americans. 18779604

2008
dbSNP: rs80357808
rs80357808
BRCA1
T 0.700 CausalMutation CLINVAR Cross-sectional analysis of germline BRCA1 and BRCA2 mutations in Japanese patients suspected to have hereditary breast/ovarian cancer. 19016756

2008