{{Rsnum
|rsid=877529
|Gene=CBX7
|Chromosome=22
|position=39146287
|Orientation=minus
|GMAF=0.3444
|Gene_s=CBX7
|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 | 32.7 | 51.3 | 15.9
| HCB | 60.6 | 35.0 | 4.4
| JPT | 68.1 | 29.2 | 2.7
| YRI | 31.3 | 48.3 | 20.4
| ASW | 31.6 | 40.4 | 28.1
| CHB | 60.6 | 35.0 | 4.4
| CHD | 62.4 | 34.9 | 2.8
| GIH | 37.6 | 55.4 | 6.9
| LWK | 39.1 | 39.1 | 21.8
| MEX | 67.2 | 24.1 | 8.6
| MKK | 34.0 | 48.1 | 17.9
| TSI | 33.3 | 54.9 | 11.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=24449210
|Title=Inherited genetic susceptibility to monoclonal gammopathy of unknown significance
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}