{{Rsnum
|rsid=3093200
|Gene=CYP4F2
|Chromosome=19
|position=15878779
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=A
|GMAF=0.05969
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=CYP4F2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.9 | 16.8 | 82.3
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.7 | 29.3 | 70.1
| ASW | 1.8 | 20.0 | 78.2
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 5.9 | 94.1
| LWK | 4.5 | 26.4 | 69.1
| MEX | 0.0 | 5.3 | 94.7
| MKK | 0.0 | 16.7 | 83.3
| TSI | 0.0 | 8.8 | 91.2
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19097922
|Title=A haplotype of the CYP4F2 gene associated with myocardial infarction in Japanese men.
}}

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

{{PMID Auto
|PMID=18971550
|Title=Haplotype-based case-control study of the human CYP4F2 gene and essential hypertension in Japanese subjects.
}}

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

{{GET Evidence
|gene=CYP4F2
|aa_change=Leu519Met
|aa_change_short=L519M
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs3093200
|overall_frequency_n=850
|overall_frequency_d=10740
|overall_frequency=0.0791434
|n_genomes=5
|n_genomes_annotated=0
|n_haplomes=5
|n_articles=0
|n_articles_annotated=0
|pph2_score=0.569
|nblosum100=-3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}