{{Rsnum
|rsid=2235121
|Gene=MYOM2
|Chromosome=8
|position=2092276
|Orientation=plus
|GMAF=0.3916
|Gene_s=MYOM2
|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 | 19.6 | 46.4 | 33.9
| HCB | 38.0 | 46.7 | 15.3
| JPT | 46.4 | 42.9 | 10.7
| YRI | 100.0 | 0.0 | 0.0
| ASW | 89.5 | 8.8 | 1.8
| CHB | 38.0 | 46.7 | 15.3
| CHD | 31.8 | 59.8 | 8.4
| GIH | 30.0 | 53.0 | 17.0
| LWK | 93.5 | 6.5 | 0.0
| MEX | 27.6 | 51.7 | 20.7
| MKK | 69.5 | 29.8 | 0.7
| TSI | 16.7 | 46.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=20889312
  |Trait=Bipolar disorder and schizophrenia
  |Title=A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.
  |RiskAllele=
  |Pval=8E-6
  |OR=1.22
  |ORtxt=[NR]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}