{{Rsnum
|rsid=1558139
|Gene=CYP4F2
|Chromosome=19
|position=15886754
|Orientation=plus
|GMAF=0.4293
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=CYP4F2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 31.9 | 44.2 | 23.9
| HCB | 14.6 | 52.6 | 32.8
| JPT | 8.0 | 43.4 | 48.7
| YRI | 8.8 | 51.0 | 40.1
| ASW | 12.3 | 57.9 | 29.8
| CHB | 14.6 | 52.6 | 32.8
| CHD | 22.0 | 42.2 | 35.8
| GIH | 31.7 | 47.5 | 20.8
| LWK | 30.0 | 49.1 | 20.9
| MEX | 15.5 | 43.1 | 41.4
| MKK | 23.1 | 53.8 | 23.1
| TSI | 15.7 | 50.0 | 34.3
| HapMapRevision=28
}}
{{PMID|18971550}} rs1558139 might be a genetic marker for EH and the T-T-G haplotype might be a protective genetic marker for essential hypertension in Japanese men.

{{PMID Auto
|PMID=19097922
|Title=A haplotype of the CYP4F2 gene associated with myocardial infarction in Japanese men.
}}

{{PMID Auto
|PMID=17903306
|Title=Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.
|OA=1
}}

{{PMID Auto
|PMID=18787519
|Title=A haplotype of the CYP4F2 gene is associated with cerebral infarction in Japanese men.
}}

{{PMID Auto
|PMID=19957603
|Title=[Association on the haplotypes of CYP4F2 gene and myocardial infarction].
}}

{{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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}