{{Rsnum
|rsid=7904463
|Gene=MSMB
|Chromosome=10
|position=51559469
|Orientation=plus
|GMAF=0.4109
|Gene_s=MSMB,TIMM23B
|Assembly=GRCh37.p2
|GenomeBuild=37.2
|dbSNPBuild=134
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 33.9 | 54.1 | 11.9
| HCB | 38.9 | 53.4 | 7.6
| JPT | 31.8 | 59.1 | 9.1
| YRI | 6.1 | 36.7 | 57.1
| ASW | 14.3 | 33.9 | 51.8
| CHB | 38.9 | 53.4 | 7.6
| CHD | 42.1 | 47.7 | 10.3
| GIH | 37.0 | 50.0 | 13.0
| LWK | 13.6 | 50.9 | 35.5
| MEX | 49.1 | 42.1 | 8.8
| MKK | 25.5 | 47.1 | 27.5
| TSI | 40.4 | 44.4 | 15.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=20717903
|Title=Evidence for an association between prostate cancer and chromosome 8q24 and 10q11 genetic variants in African American men: The flint men's health study
}}

{{PMID Auto
|PMID=19383797
|Title=Fine mapping and functional analysis of a common variant in MSMB on chromosome 10q11.2 associated with prostate cancer susceptibility.
|OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | Illumina Human 1M}}