{{Rsnum
|rsid=6107516
|Gene=PRNP
|Chromosome=20
|position=4696446
|Orientation=plus
|GMAF=0.1869
|Gene_s=PRNP
|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 | 8.8 | 31.0 | 60.2
| HCB | 0.7 | 5.8 | 93.4
| JPT | 0.0 | 0.9 | 99.1
| YRI | 4.8 | 28.8 | 66.4
| ASW | 5.3 | 29.8 | 64.9
| CHB | 0.7 | 5.8 | 93.4
| CHD | 0.0 | 0.9 | 99.1
| GIH | 3.0 | 25.7 | 71.3
| LWK | 2.7 | 36.4 | 60.9
| MEX | 8.6 | 34.5 | 56.9
| MKK | 10.3 | 32.7 | 57.1
| TSI | 4.9 | 41.2 | 53.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22137330
|Trait=None
|Title=Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
|RiskAllele=
|Pval=3E-18
|OR=None
|ORtxt=None
}}

{{PMID Auto
|PMID=19081515
|Title=Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.
|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 | FTDNA}}
{{on chip | Illumina Human 1M}}