{{Rsnum
|rsid=7656250
|Gene=PPARGC1A
|Chromosome=4
|position=23864393
|Orientation=plus
|GMAF=0.2654
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PPARGC1A
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 7.1 | 38.1 | 54.9
| HCB | 13.9 | 44.5 | 41.6
| JPT | 12.4 | 57.5 | 30.1
| YRI | 0.7 | 13.6 | 85.7
| ASW | 1.8 | 21.1 | 77.2
| CHB | 13.9 | 44.5 | 41.6
| CHD | 15.6 | 38.5 | 45.9
| GIH | 12.9 | 54.5 | 32.7
| LWK | 0.0 | 13.6 | 86.4
| MEX | 3.5 | 50.9 | 45.6
| MKK | 0.6 | 22.4 | 76.9
| TSI | 6.9 | 48.0 | 45.1
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19183932
|Title=PPARGC1A sequence variation and cardiovascular risk-factor levels: a study of the main genetic effects and gene x environment interactions in children from the European Youth Heart Study
}}

{{PMID Auto
|PMID=19828207
|Title=Evaluation of the association between the PPARGC1A genetic polymorphisms and type 2 diabetes in Han Chinese population
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}