{{Rsnum
|rsid=32582
|Gene=PPARGC1B
|Chromosome=5
|position=149825854
|Orientation=plus
|GMAF=0.2057
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=PPARGC1B
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 67.0 | 30.4 | 2.7
| HCB | 64.2 | 33.6 | 2.2
| JPT | 69.9 | 27.4 | 2.7
| YRI | 51.7 | 42.9 | 5.4
| ASW | 61.4 | 29.8 | 8.8
| CHB | 64.2 | 33.6 | 2.2
| CHD | 61.5 | 32.1 | 6.4
| GIH | 44.6 | 49.5 | 5.9
| LWK | 57.3 | 36.4 | 6.4
| MEX | 82.8 | 15.5 | 1.7
| MKK | 67.3 | 28.2 | 4.5
| TSI | 72.5 | 26.5 | 1.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=20937954
|Title=Mapping of Autosomal Dominant Cerebellar Ataxia Without the Pathogenic PPP2R2B Mutation to the Locus for Spinocerebellar Ataxia 12
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}