{{Rsnum
|rsid=6821591
|Gene=PPARGC1A
|Chromosome=4
|position=23795377
|Orientation=plus
|GMAF=0.4229
|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 | 23.0 | 49.6 | 27.4
| HCB | 8.0 | 42.3 | 49.6
| JPT | 8.0 | 40.7 | 51.3
| YRI | 14.3 | 43.5 | 42.2
| ASW | 19.3 | 56.1 | 24.6
| CHB | 8.0 | 42.3 | 49.6
| CHD | 9.2 | 41.3 | 49.5
| GIH | 11.9 | 42.6 | 45.5
| LWK | 10.1 | 49.5 | 40.4
| MEX | 31.0 | 50.0 | 19.0
| MKK | 7.1 | 35.9 | 57.1
| TSI | 14.7 | 54.9 | 30.4
| HapMapRevision=28
}}{{PMID Auto
|PMID=21595954
|Title=Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease
|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 | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}