Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1049112
rs1049112
PRH1 ; PRH2 ; PRR4 ; PRH1-PRR4
0.010 GeneticVariation BEFREE On the other hand, AG and GA haplotypes of 2 CCL4 SNPs (rs1049112 and rs171915) also reduced the risks for HCC by 0.025 and 0.515 fold, respectively. 28824325

2017