{{Rsnum
|rsid=12761224
|Chromosome=10
|position=72527517
|Orientation=plus
|GMAF=0.07713
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 77.9 | 20.4 | 1.8
| HCB | 70.8 | 27.7 | 1.5
| JPT | 89.4 | 9.7 | 0.9
| YRI | 100.0 | 0.0 | 0.0
| ASW | 94.7 | 5.3 | 0.0
| CHB | 70.8 | 27.7 | 1.5
| CHD | 80.7 | 19.3 | 0.0
| GIH | 83.2 | 15.8 | 1.0
| LWK | 99.1 | 0.9 | 0.0
| MEX | 84.5 | 15.5 | 0.0
| MKK | 89.7 | 10.3 | 0.0
| TSI | 87.3 | 12.7 | 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=0.000006
|OR=1.3861
|ORtxt=None
|OA=1
}}

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