Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135519
rs1135519
0.010 GeneticVariation BEFREE Our results suggest that SNP of rs1135519 modulates <i>miR-122</i> expression and contributes to the genetic susceptibility of HCC, either independently or together with rs9966765 in <i>miR-122.</i> Further well-designed studies with lager sample sizes are needed to confirm our findings. 30662901

2018

dbSNP: rs17669
rs17669
0.010 GeneticVariation BEFREE Three selected SNPs in <i>miR-122</i> (rs9966765, rs1135519, and rs17669) were genotyped in 1050 HCC patients and 1079 cancer-free controls using Sequenom MassARRAY platform and the associations of the three SNPs and HCC risk were evaluated. 30662901

2018

dbSNP: rs9966765
rs9966765
0.010 GeneticVariation BEFREE There was also a significant increased risk of HCC when combining risk genotypes of these loci, i.e., rs1135519 CC and rs9966765 CC. 30662901

2018