Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80359438
rs80359438
BRCA2
TA 0.700 CausalMutation CLINVAR Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels. 28152038

2017
dbSNP: rs80359438
rs80359438
BRCA2
TA 0.700 CausalMutation CLINVAR Cancer variation associated with the position of the mutation in the BRCA2 gene. 15131399

2004