Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80356962
rs80356962
BRCA1
T 0.700 CausalMutation CLINVAR Hereditary breast and ovarian cancer: assessment of point mutations and copy number variations in Brazilian patients. 24884479

2014
dbSNP: rs80356962
rs80356962
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer. 15365993

2004
dbSNP: rs80356962
rs80356962
BRCA1
T 0.700 CausalMutation CLINVAR Germline mutations of BRCA1 and BRCA2 in Korean breast and/or ovarian cancer families. 12204006

2002
dbSNP: rs80356962
rs80356962
BRCA1
T 0.700 CausalMutation CLINVAR Identification of seven new BRCA1 germline mutations in Italian breast and breast/ovarian cancer families. 8968102

1996