{{Rsnum
|rsid=17036170
|Gene=PPARG
|Chromosome=3
|position=12288912
|Orientation=plus
|GMAF=0.009183
|Gene_s=PPARG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{PMID Auto GWAS
  |PMID=22968431
  |Trait=Drug-induced liver injury
  |Title=Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.
  |RiskAllele=
  |Pval=2E-8
  |OR=11.30
  |ORtxt=[4.9-25.9]
  |OA=1
}}

{{ population diversity
| geno1 = (A;G)
| geno2 = (G;G)
| geno3 = 
| CEU | 0.9 | 99.1 | 0
| HCB | 0 | 0 | 0
| JPT | 0 | 0 | 0
| YRI | 0 | 0 | 0
| ASW | 2.0 | 98.0 | 0
| CHD | 0 | 0 | 0
| GIH | 0 | 0 | 0
| LWK | 0 | 0 | 0
| MEX | 6.0 | 94.0 | 0
| MKK | 0 | 0 | 0
| TSI | 6.8 | 93.2 | 0
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}