{{Rsnum
|rsid=2970869
|Gene=PPARGC1A
|Chromosome=4
|position=23891746
|Orientation=minus
|GMAF=0.2525
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=PPARGC1A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.4 | 34.2 | 60.4
| HCB | 14.5 | 39.7 | 45.8
| JPT | 31.8 | 36.4 | 31.8
| YRI | 0.0 | 4.8 | 95.2
| ASW | 0.0 | 11.1 | 88.9
| CHB | 14.5 | 39.7 | 45.8
| CHD | 16.3 | 47.1 | 36.5
| GIH | 2.0 | 39.8 | 58.2
| LWK | 0.0 | 0.0 | 0.0
| MEX | 39.7 | 44.8 | 15.5
| MKK | 0.0 | 14.8 | 85.2
| TSI | 4.1 | 32.7 | 63.3
| 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=18162502
|Title=PPARGC1A variation associated with DNA damage, diabetes, and cardiovascular diseases: the Boston Puerto Rican Health Study.
|OA=1
}}

{{PMID Auto
|PMID=19200361
|Title=PGC-1alpha as modifier of onset age in Huntington disease.
|OA=1
}}

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