{{Rsnum
|rsid=3755863
|Gene=PPARGC1A
|Chromosome=4
|position=23813899
|Orientation=minus
|GMAF=0.371
|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 | 17.7 | 46.9 | 35.4
| HCB | 18.5 | 45.9 | 35.6
| JPT | 27.4 | 51.3 | 21.2
| YRI | 5.5 | 31.7 | 62.8
| ASW | 1.8 | 45.6 | 52.6
| CHB | 18.5 | 45.9 | 35.6
| CHD | 14.7 | 52.3 | 33.0
| GIH | 13.9 | 48.5 | 37.6
| LWK | 10.1 | 34.9 | 55.0
| MEX | 8.8 | 43.9 | 47.4
| MKK | 8.3 | 42.3 | 49.4
| TSI | 22.5 | 53.9 | 23.5
| 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=20125101
|Title=Glucose levels and genetic variants across transcriptional pathways: interaction effects with BMI
}}

{{PMID Auto
|PMID=18588668
|Title=Association between PPARGC1A polymorphisms and the occurrence of nonalcoholic fatty liver disease (NAFLD).
|OA=1
}}

{{PMID Auto
|PMID=19133136
|Title=The gene coding for PGC-1alpha modifies age at onset in Huntington's Disease.
|OA=1
}}

{{PMID Auto
|PMID=21211002
|Title=Localization of sequence variations in PGC-1alpha influence their modifying effect in Huntington disease.
|OA=1
}}

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