{{Rsnum
|rsid=6031882
|Gene=RPN2
|Chromosome=20
|position=37181380
|Orientation=plus
|GMAF=0.3297
|Gene_s=C20orf132,RPN2
|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 | 13.3 | 39.8 | 46.9
| HCB | 0.0 | 5.1 | 94.9
| JPT | 0.0 | 1.8 | 98.2
| YRI | 26.5 | 54.4 | 19.0
| ASW | 47.4 | 42.1 | 10.5
| CHB | 0.0 | 5.1 | 94.9
| CHD | 0.0 | 4.6 | 95.4
| GIH | 9.0 | 54.0 | 37.0
| LWK | 43.6 | 44.5 | 11.8
| MEX | 6.9 | 27.6 | 65.5
| MKK | 25.6 | 53.2 | 21.2
| TSI | 14.7 | 52.9 | 32.4
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19668339
|Trait=Hippocampal atrophy
|Title=Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease
|RiskAllele=
|Pval=0.000006
|OR=NR
|ORtxt=NR
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6031882
|overall_frequency_n=53
|overall_frequency_d=128
|overall_frequency=0.414062
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=43
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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