{{Rsnum
|rsid=2712381
|Gene=RPN1
|Chromosome=3
|position=128619757
|Orientation=minus
|GMAF=0.337
|Gene_s=RPN1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 37.2 | 46.0 | 16.8
| HCB | 56.9 | 36.5 | 6.6
| JPT | 66.4 | 29.2 | 4.4
| YRI | 36.7 | 46.3 | 17.0
| ASW | 50.9 | 38.6 | 10.5
| CHB | 56.9 | 36.5 | 6.6
| CHD | 62.4 | 33.0 | 4.6
| GIH | 24.8 | 55.4 | 19.8
| LWK | 48.2 | 39.1 | 12.7
| MEX | 32.8 | 44.8 | 22.4
| MKK | 42.3 | 46.2 | 11.5
| TSI | 45.1 | 49.0 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23314186
  |Trait=Monocyte count
  |Title=Genetic variation associated with circulating monocyte count in the eMERGE Network.
  |RiskAllele=A
  |Pval=2E-16
  |OR=.23
  |ORtxt=unit decrease
  |OA=1
}}

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