{{Rsnum
|rsid=2903698
|Chromosome=4
|position=75407765
|Orientation=plus
|GMAF=0.1566
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 48.7 | 38.9 | 12.4
| HCB | 91.2 | 8.0 | 0.7
| JPT | 79.5 | 19.6 | 0.9
| YRI | 84.4 | 15.0 | 0.7
| ASW | 80.7 | 15.8 | 3.5
| CHB | 91.2 | 8.0 | 0.7
| CHD | 82.6 | 17.4 | 0.0
| GIH | 69.3 | 28.7 | 2.0
| LWK | 84.5 | 13.6 | 1.8
| MEX | 79.3 | 17.2 | 3.4
| MKK | 84.0 | 14.7 | 1.3
| TSI | 67.6 | 26.5 | 5.9
| 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=1.2528
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}