{{Rsnum
|rsid=12636454
|Gene=PPARG
|Chromosome=3
|position=12318715
|Orientation=plus
|GMAF=0.2856
|Gene_s=PPARG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 5.3 | 35.4 | 59.3
| HCB | 15.3 | 40.1 | 44.5
| JPT | 10.7 | 33.0 | 56.2
| YRI | 9.0 | 40.3 | 50.7
| ASW | 8.8 | 47.4 | 43.9
| CHB | 15.3 | 40.1 | 44.5
| CHD | 12.8 | 44.0 | 43.1
| GIH | 4.0 | 38.6 | 57.4
| LWK | 9.2 | 32.1 | 58.7
| MEX | 17.2 | 48.3 | 34.5
| MKK | 15.7 | 45.1 | 39.2
| TSI | 4.9 | 38.2 | 56.9
| HapMapRevision=28
}}{{PMID Auto
|PMID=23386649
|Title=Common Genetic Variants in Peroxisome Proliferator-Activated Receptor-γ (PPARG) and Type 2 Diabetes Risk Among Women's Health Initiative Postmenopausal Women
|OA=1
}}

{{PMID Auto
|PMID=20550665
|Title=Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}