{{Rsnum
|rsid=1016342
|Chromosome=8
|position=127080210
|Orientation=plus
|GMAF=0.4614
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PRNCR1
|Gene_s=PRNCR1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.4 | 50.0 | 19.6
| HCB | 17.5 | 46.7 | 35.8
| JPT | 12.4 | 40.7 | 46.9
| YRI | 12.2 | 41.5 | 46.3
| ASW | 3.5 | 57.9 | 38.6
| CHB | 17.5 | 46.7 | 35.8
| CHD | 15.6 | 48.6 | 35.8
| GIH | 37.6 | 54.5 | 7.9
| LWK | 7.3 | 33.6 | 59.1
| MEX | 43.1 | 50.0 | 6.9
| MKK | 18.6 | 42.9 | 38.5
| TSI | 32.0 | 46.0 | 22.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19562729
|Title=Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry
|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}}