Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397509141
rs397509141
BRCA1
C 0.700 CausalMutation CLINVAR The role of targeted BRCA1/BRCA2 mutation analysis in hereditary breast/ovarian cancer families of Portuguese ancestry. 24916970

2015
dbSNP: rs397509141
rs397509141
BRCA1
C 0.700 CausalMutation CLINVAR BRCA1 germline mutations in Chinese patients with hereditary breast and ovarian cancer. 16515586

2006