{{Rsnum
|rsid=7578982
|Gene=ACOXL
|Chromosome=2
|position=111078961
|Orientation=plus
|GMAF=0.3044
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=ACOXL
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 11.5 | 43.4 | 45.1
| HCB | 21.5 | 46.7 | 31.9
| JPT | 14.3 | 55.4 | 30.4
| YRI | 4.1 | 25.5 | 70.3
| ASW | 12.3 | 19.3 | 68.4
| CHB | 21.5 | 46.7 | 31.9
| CHD | 22.2 | 50.0 | 27.8
| GIH | 1.0 | 30.0 | 69.0
| LWK | 2.7 | 24.5 | 72.7
| MEX | 12.1 | 41.4 | 46.6
| MKK | 3.9 | 23.9 | 72.3
| TSI | 5.9 | 46.1 | 48.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21738478
|Trait=None
|Title=Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population.
|RiskAllele=T
|Pval=4E-7
|OR=0.0540
|ORtxt=[0.03-0.07] unit increase
|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}}