Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357848
rs80357848
BRCA1
GT 0.700 CausalMutation CLINVAR Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing. 26681312

2016
dbSNP: rs80357848
rs80357848
BRCA1
GT 0.700 CausalMutation CLINVAR Recurrent germ-line BRCA1 mutations in extended African American families with early-onset breast cancer. 9150171

1997