Gene: IGF2R ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121434587
rs121434587
IGF2R
T 0.700 CausalMutation CLINVAR

dbSNP: rs121434588
rs121434588
IGF2R
A 0.700 CausalMutation CLINVAR

dbSNP: rs629849
rs629849
IGF2R
0.010 GeneticVariation BEFREE The IGF2R SNPs rs629849 and rs642588 were not significantly associated with HCC risk, whereas a homozygous IGF2R rs629849 GG genotype was associated with a significantly elevated risk of non‑viral liver cirrhosis (P=0.05). 30720132

2019
dbSNP: rs642588
rs642588
IGF2R
0.010 GeneticVariation BEFREE The IGF2R SNPs rs629849 and rs642588 were not significantly associated with HCC risk, whereas a homozygous IGF2R rs629849 GG genotype was associated with a significantly elevated risk of non‑viral liver cirrhosis (P=0.05). 30720132

2019