{{Rsnum
|rsid=253959
|Gene=COMMD10
|Chromosome=5
|position=116233060
|Orientation=plus
|GMAF=0.4656
|Gene_s=COMMD10
|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 | 12.4 | 36.3 | 51.3
| HCB | 35.0 | 48.2 | 16.8
| JPT | 39.8 | 51.3 | 8.8
| YRI | 89.8 | 10.2 | 0.0
| ASW | 68.4 | 24.6 | 7.0
| CHB | 35.0 | 48.2 | 16.8
| CHD | 44.0 | 45.9 | 10.1
| GIH | 12.9 | 59.4 | 27.7
| LWK | 82.7 | 17.3 | 0.0
| MEX | 15.5 | 48.3 | 36.2
| MKK | 52.6 | 41.0 | 6.4
| TSI | 15.7 | 38.2 | 46.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22688191
|Trait=None
|Title=Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
|RiskAllele=T
|Pval=0.000008
|OR=1.2100
|ORtxt=None
|OA=1
}}

{{on chip | Illumina Human 1M}}