{{Rsnum
|rsid=12570947
|Chromosome=10
|position=109569850
|Orientation=plus
|GMAF=0.2672
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.0 | 11.1 | 88.9
| HCB | 25.9 | 43.7 | 30.4
| JPT | 23.9 | 54.9 | 21.2
| YRI | 3.2 | 33.9 | 62.9
| ASW | 0.0 | 0.0 | 0.0
| CHB | 25.9 | 43.7 | 30.4
| CHD | 24.1 | 42.6 | 33.3
| GIH | 0.0 | 0.0 | 0.0
| LWK | 6.5 | 38.0 | 55.6
| MEX | 3.6 | 36.4 | 60.0
| MKK | 6.5 | 39.2 | 54.2
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22210626
|Trait=None
|Title=Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
|RiskAllele=
|Pval=0.000004
|OR=1.4500
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}