{{Rsnum
|rsid=17587
|Gene=PSMB9
|Chromosome=6
|position=32857313
|Orientation=plus
|GMAF=0.2231
|Gene_s=PSMB9
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 5.3 | 39.8 | 54.9
| HCB | 2.2 | 38.0 | 59.9
| JPT | 6.2 | 32.7 | 61.1
| YRI | 3.4 | 39.5 | 57.1
| ASW | 5.3 | 35.1 | 59.6
| CHB | 2.2 | 38.0 | 59.9
| CHD | 7.3 | 27.5 | 65.1
| GIH | 3.0 | 36.6 | 60.4
| LWK | 1.8 | 27.3 | 70.9
| MEX | 6.9 | 31.0 | 62.1
| MKK | 4.5 | 32.1 | 63.5
| TSI | 5.9 | 42.2 | 52.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=22034108
|Title=Radiographic severity in ankylosing spondylitis is associated with polymorphism in large multifunctional peptidase 2 (LMP2) in the SPARCC cohort
}}

{{PMID Auto
|PMID=12830434
|Title=BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.
|OA=1
}}

{{GET Evidence
|gene=PSMB9
|aa_change=Arg60His
|aa_change_short=R60H
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17587
|overall_frequency_n=29
|overall_frequency_d=126
|overall_frequency=0.230159
|n_genomes=21
|n_genomes_annotated=0
|n_haplomes=22
|n_articles=0
|n_articles_annotated=0
|nblosum100=1
|autoscore=0
|webscore=N
}}

{{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}}