{{Rsnum
|rsid=10207392
|Gene=ACOXL
|Chromosome=2
|position=111092082
|Orientation=plus
|GMAF=0.4858
|Gene_s=ACOXL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 27.4 | 46.0 | 26.5
| HCB | 20.4 | 56.9 | 22.6
| JPT | 20.4 | 61.1 | 18.6
| YRI | 17.7 | 46.3 | 36.1
| ASW | 21.1 | 42.1 | 36.8
| CHB | 20.4 | 56.9 | 22.6
| CHD | 21.1 | 50.5 | 28.4
| GIH | 36.6 | 46.5 | 16.8
| LWK | 15.5 | 44.5 | 40.0
| MEX | 21.1 | 63.2 | 15.8
| MKK | 10.3 | 48.1 | 41.7
| TSI | 27.5 | 52.9 | 19.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23222517
  |Trait=Red blood cell traits
  |Title=Seventy-five genetic loci influencing the human red blood cell.
  |RiskAllele=G
  |Pval=4E-11
  |OR=.13
  |ORtxt=[0.083-0.181] unit decrease
  |OA=1
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}