{{Rsnum
|rsid=2071598
|Gene=HRSP12
|Chromosome=8
|position=98117279
|Orientation=minus
|GMAF=0.1869
|Gene_s=HRSP12,POP1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 8.8 | 32.7 | 58.4
| HCB | 0.0 | 16.2 | 83.8
| JPT | 2.7 | 31.0 | 66.4
| YRI | 2.0 | 30.6 | 67.3
| ASW | 7.0 | 35.1 | 57.9
| CHB | 0.0 | 16.2 | 83.8
| CHD | 0.0 | 16.5 | 83.5
| GIH | 1.0 | 37.6 | 61.4
| LWK | 2.7 | 29.1 | 68.2
| MEX | 5.2 | 36.2 | 58.6
| MKK | 0.6 | 21.8 | 77.6
| TSI | 4.9 | 19.6 | 75.5
| 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=0.000009
|OR=1.2646
|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}}