Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397508838
rs397508838
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 germline mutations in Chinese patients with hereditary breast and ovarian cancer. 16515586

2006
dbSNP: rs397508838
rs397508838
BRCA1
T 0.700 CausalMutation CLINVAR BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing. 9333265

1997