rs3856806, PPARG

N. diseases: 41
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
0.010 GeneticVariation BEFREE However, <i>PPARG</i> rs3856806 C>T polymorphism was a risk factor for HCC (TT vs CC, adjusted OR 2.33, 95% CI 1.25-4.36, <i>P</i>=0.008; TT vs CT/CC, adjusted OR 2.26, 95% CI 1.22-4.17, <i>P</i>=0.010). 30122956 2018