{{Rsnum
|rsid = 1137582
|Status = Merged
|Merged = 1135640
|Gene = ACOX1
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=G
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Chromosome=17
|position=75953459
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ACOX1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 12.4 | 46.0 | 41.6
| HCB | 6.6 | 28.5 | 65.0
| JPT | 9.7 | 43.4 | 46.9
| YRI | 74.8 | 25.2 | 0.0
| ASW | 66.7 | 24.6 | 8.8
| CHB | 6.6 | 28.5 | 65.0
| CHD | 0.9 | 37.0 | 62.0
| GIH | 10.9 | 34.7 | 54.5
| LWK | 70.0 | 27.3 | 2.7
| MEX | 14.3 | 44.6 | 41.1
| MKK | 53.8 | 36.5 | 9.6
| TSI | 16.7 | 51.0 | 32.4
| HapMapRevision=28
}}{{Venter SNP
|rsid=1137582
|allele=C
|frequency=0.65
|uid=1103645382811
|type=homozygous_SNP
|hugo=ACOX1
|ensembl gene=ENSG00000161533
|ensembl transcript=ENST00000301608
|sift=
|disease=Defects in ACOX1 are the cause of pseudoneonatal adrenoleukodystrophy (MIM:264470). It is a disease biochemically characterized by an accumulation of very long chain fatty acids.
}}

{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}