Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776665
rs587776665
C 0.700 CausalMutation CLINVAR

dbSNP: rs3834129
rs3834129
0.010 GeneticVariation BEFREE Among the 11 polymorphisms, only CASP8 rs3834129 (-652 6N ins/del) modified HCC risk. 28643196

2017