{{Rsnum
|rsid=7657071
|Chromosome=4
|position=23894851
|Orientation=plus
|GMAF=0.2502
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PPARGC1A
|Gene_s=PPARGC1A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 12.4 | 46.0 | 41.6
| HCB | 0.7 | 19.7 | 79.6
| JPT | 1.8 | 12.5 | 85.7
| YRI | 8.2 | 41.5 | 50.3
| ASW | 5.4 | 44.6 | 50.0
| CHB | 0.7 | 19.7 | 79.6
| CHD | 0.9 | 24.1 | 75.0
| GIH | 3.0 | 34.7 | 62.4
| LWK | 7.4 | 43.5 | 49.1
| MEX | 3.4 | 27.6 | 69.0
| MKK | 4.5 | 29.5 | 66.0
| TSI | 22.5 | 32.4 | 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
}}

{{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}}