{{Rsnum
|rsid=3934861
|Gene=MYOM3
|Chromosome=1
|position=24105466
|Orientation=minus
|GMAF=0.4986
|Gene_s=MYOM3
|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 | 27.4 | 51.3 | 21.2
| HCB | 45.3 | 42.3 | 12.4
| JPT | 53.1 | 34.5 | 12.4
| YRI | 11.6 | 38.8 | 49.7
| ASW | 10.5 | 47.4 | 42.1
| CHB | 45.3 | 42.3 | 12.4
| CHD | 38.5 | 43.1 | 18.3
| GIH | 33.7 | 48.5 | 17.8
| LWK | 11.8 | 45.5 | 42.7
| MEX | 43.1 | 36.2 | 20.7
| MKK | 10.3 | 55.8 | 34.0
| TSI | 29.4 | 47.1 | 23.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23092984
  |Trait=Bipolar disorder (mood-incongruent)
  |Title=Genome-wide association of mood-incongruent psychotic bipolar disorder.
  |RiskAllele=
  |Pval=4E-6
  |OR=1.25
  |ORtxt=[NR]
  |OA=1
}}

{{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}}