{{Rsnum
|rsid=433598
|Gene=ACSM1
|Chromosome=16
|position=20668884
|Orientation=plus
|GMAF=0.4096
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ACSM1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 46.0 | 44.2 | 9.7
| HCB | 1.5 | 16.8 | 81.8
| JPT | 1.8 | 10.6 | 87.6
| YRI | 3.4 | 32.0 | 64.6
| ASW | 10.5 | 47.4 | 42.1
| CHB | 1.5 | 16.8 | 81.8
| CHD | 2.8 | 30.3 | 67.0
| GIH | 15.8 | 48.5 | 35.6
| LWK | 5.5 | 31.8 | 62.7
| MEX | 43.1 | 48.3 | 8.6
| MKK | 10.3 | 48.7 | 41.0
| TSI | 34.3 | 52.0 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20185149
|Trait=Schizophrenia
|Title=Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.
|RiskAllele=T
|Pval=0.000003
|OR=1.13
|ORtxt=[NR]
|OA=1
}}

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