{{Rsnum
|rsid=295301
|Chromosome=3
|position=141619799
|Orientation=plus
|GMAF=0.3866
|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 | 12.3 | 49.2 | 38.5
| HCB | 11.2 | 41.8 | 47.0
| JPT | 12.8 | 41.3 | 45.9
| YRI | 20.6 | 45.4 | 34.0
| ASW | 25.0 | 60.7 | 14.3
| CHB | 11.2 | 41.8 | 47.0
| CHD | 14.3 | 55.2 | 30.5
| GIH | 11.2 | 52.0 | 36.7
| LWK | 28.0 | 44.9 | 27.1
| MEX | 12.5 | 42.9 | 44.6
| MKK | 33.6 | 48.7 | 17.8
| TSI | 6.0 | 46.0 | 48.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22210626
|Title=Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP
|OA=1
}}

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