{{Rsnum
|rsid=155100
|Gene=ITGA4
|Chromosome=2
|position=181485360
|Orientation=minus
|GMAF=0.4229
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=ITGA4
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 16.9 | 46.2 | 36.9
| HCB | 20.0 | 42.2 | 37.8
| JPT | 25.0 | 43.2 | 31.8
| YRI | 22.2 | 49.2 | 28.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 20.0 | 42.2 | 37.8
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=19259978
|Title=Association of the alpha4 integrin subunit gene (ITGA4) with autism
}}

{{PMID Auto
|PMID=14681825
|Title=Mutation of CERKL, a novel human ceramide kinase gene, causes autosomal recessive retinitis pigmentosa (RP26).
|OA=1
}}

{{PMID Auto
|PMID=18806881
|Title=Identification of candidate regions for a novel Usher syndrome type II locus.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}