{{Rsnum
|rsid=1126667
|Gene=ALOX12
|Chromosome=17
|position=6999441
|Orientation=plus
|GMAF=0.3884
|Gene_s=ALOX12
|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 | 23.4 | 40.5 | 36.0
| HCB | 19.1 | 54.4 | 26.5
| JPT | 17.0 | 55.4 | 27.7
| YRI | 10.9 | 41.5 | 47.6
| ASW | 14.0 | 36.8 | 49.1
| CHB | 19.1 | 54.4 | 26.5
| CHD | 25.9 | 51.9 | 22.2
| GIH | 31.7 | 41.6 | 26.7
| LWK | 9.2 | 38.5 | 52.3
| MEX | 8.9 | 55.4 | 35.7
| MKK | 18.6 | 41.0 | 40.4
| TSI | 14.7 | 45.1 | 40.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=21104233
|Title=Polymorphisms in the ALOX12 gene and osteoporosis
}}

{{PMID Auto
|PMID=18640486
|Title=Association of arachidonate 12-lipoxygenase genotype variation and glycemic control with albuminuria in type 2 diabetes.
|OA=1
}}

{{PMID Auto
|PMID=18992148
|Title=Low-penetrance alleles predisposing to sporadic colorectal cancers: a French case-controlled genetic association study.
|OA=1
}}

{{PMID Auto
|PMID=19774229
|Title=The relationship of DNA methylation with age, gender and genotype in twins and healthy controls.
|OA=1
}}

{{PMID Auto
|PMID=20626912
|Title=Association between polymorphisms of arachidonate 12-lipoxygenase (ALOX12) and schizophrenia in a Korean population.
|OA=1
}}

{{GET Evidence
|gene=ALOX12
|aa_change=Gln261Arg
|aa_change_short=Q261R
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1126667
|overall_frequency_n=6514
|overall_frequency_d=10758
|overall_frequency=0.605503
|n_genomes=49
|n_genomes_annotated=0
|n_haplomes=76
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{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}}