{{Rsnum
|rsid=2228064
|Gene=ALOX5
|Chromosome=10
|position=45878050
|Orientation=plus
|GMAF=0.1019
|Gene_s=ALOX5
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.0 | 0.9 | 99.1
| HCB | 1.5 | 13.1 | 85.4
| JPT | 0.9 | 11.5 | 87.6
| YRI | 12.9 | 50.3 | 36.7
| ASW | 10.5 | 33.3 | 56.1
| CHB | 1.5 | 13.1 | 85.4
| CHD | 0.0 | 11.9 | 88.1
| GIH | 0.0 | 4.0 | 96.0
| LWK | 14.5 | 40.9 | 44.5
| MEX | 1.7 | 6.9 | 91.4
| MKK | 0.6 | 16.0 | 83.3
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}{{PMID Auto
|PMID=21816595
|Title=A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population
}}

{{PMID Auto
|PMID=18248681
|Title=Prevalence of common disease-associated variants in Asian Indians.
|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}}