{{Rsnum
|rsid=2660899
|Gene=LTA4H
|Chromosome=12
|position=96036642
|Orientation=plus
|GMAF=0.2691
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=LTA4H
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 67.3 | 28.3 | 4.4
| HCB | 37.5 | 50.0 | 12.5
| JPT | 24.1 | 46.4 | 29.5
| YRI | 83.0 | 16.3 | 0.7
| ASW | 71.9 | 22.8 | 5.3
| CHB | 37.5 | 50.0 | 12.5
| CHD | 30.8 | 48.6 | 20.6
| GIH | 65.0 | 31.0 | 4.0
| LWK | 67.0 | 29.4 | 3.7
| MEX | 36.2 | 43.1 | 20.7
| MKK | 61.3 | 32.9 | 5.8
| TSI | 54.9 | 39.2 | 5.9
| HapMapRevision=28
}}Despite earlier reports of an association, no risk for [[myocardial infarction]] was seen for [[rs2660899]] variants in a study of 1,211 German patients. {{PMID|18318662}}

{{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}}