{{Rsnum
|rsid=805264
|Gene=APOM
|Chromosome=6
|position=31656096
|Orientation=minus
|GMAF=0.07254
|Gene_s=APOM
|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 | 96.5 | 3.5 | 0.0
| HCB | 73.0 | 24.8 | 2.2
| JPT | 89.4 | 8.0 | 2.7
| YRI | 72.1 | 22.4 | 5.4
| ASW | 71.9 | 26.3 | 1.8
| CHB | 73.0 | 24.8 | 2.2
| CHD | 67.9 | 30.3 | 1.8
| GIH | 92.1 | 7.9 | 0.0
| LWK | 77.3 | 20.9 | 1.8
| MEX | 89.7 | 10.3 | 0.0
| MKK | 84.6 | 14.7 | 0.6
| TSI | 93.1 | 6.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21390319
|Title=Apolipoprotein M gene (APOM) polymorphism modifies metabolic and disease traits in type 2 diabetes.
|OA=1
}}
C allele of rs805297 was significantly associated with T2D duration of longer than 10 years (OR?=?1.245, p?=?0.015).

{{PMID Auto
|PMID=17557255
|Title=[Distribution characters and linkage disequilibrium analysis of APOM gene polymorphisms in Han population of North China].
}}

{{PMID Auto
|PMID=19932739
|Title=WITHDRAWN: Association of apolipoprotein M gene polymorphisms with cerebral infarction and lipid levels in a Chinese Han population.
}}

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