{{Rsnum
|rsid=681591
|Gene=PRELID2
|Chromosome=5
|position=145832582
|Orientation=plus
|GMAF=0.4302
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=PRELID2
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 10.6 | 45.1 | 44.2
| HCB | 34.3 | 44.5 | 21.2
| JPT | 32.7 | 48.7 | 18.6
| YRI | 32.7 | 51.7 | 15.6
| ASW | 19.3 | 64.9 | 15.8
| CHB | 34.3 | 44.5 | 21.2
| CHD | 30.3 | 43.1 | 26.6
| GIH | 7.9 | 50.5 | 41.6
| LWK | 30.9 | 46.4 | 22.7
| MEX | 12.1 | 41.4 | 46.6
| MKK | 10.3 | 41.3 | 48.4
| TSI | 11.8 | 39.2 | 49.0
| 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 | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}