{{Rsnum
|rsid=2756271
|Gene=PRNP
|Chromosome=20
|position=4684616
|Orientation=minus
|GMAF=0.4123
|Gene_s=PRNP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 36.3 | 51.3 | 12.4
| HCB | 20.4 | 46.7 | 32.8
| JPT | 19.5 | 41.6 | 38.9
| YRI | 38.1 | 52.4 | 9.5
| ASW | 50.9 | 42.1 | 7.0
| CHB | 20.4 | 46.7 | 32.8
| CHD | 15.6 | 42.2 | 42.2
| GIH | 25.7 | 49.5 | 24.8
| LWK | 39.1 | 45.5 | 15.5
| MEX | 55.2 | 36.2 | 8.6
| MKK | 31.4 | 39.1 | 29.5
| TSI | 31.4 | 44.1 | 24.5
| HapMapRevision=28
}}{{PMID Auto
|PMID=22561193
|Title=Genotype patterns and characteristics of PRNP in the Korean population
|OA=1
}}

{{PMID Auto
|PMID=18347820
|Title=Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}