{{Rsnum
|rsid=4849121
|Gene=ACOXL
|Chromosome=2
|position=110842129
|Orientation=plus
|GMAF=0.4747
|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 | 20.4 | 51.3 | 28.3
| HCB | 35.0 | 43.8 | 21.2
| JPT | 37.2 | 39.8 | 23.0
| YRI | 7.5 | 43.5 | 49.0
| ASW | 7.0 | 40.4 | 52.6
| CHB | 35.0 | 43.8 | 21.2
| CHD | 35.8 | 43.1 | 21.1
| GIH | 22.8 | 46.5 | 30.7
| LWK | 15.5 | 50.9 | 33.6
| MEX | 25.9 | 56.9 | 17.2
| MKK | 25.0 | 51.3 | 23.7
| TSI | 20.6 | 53.9 | 25.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22197929
|Trait=None
|Title=A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy.
|RiskAllele=G
|Pval=4E-7
|OR=1.1500
|ORtxt=None
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}