{{Rsnum
|rsid=3794987
|Gene=CYP4F3
|Chromosome=19
|position=15640081
|Orientation=minus
|GMAF=0.3843
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=CYP4F3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 32.7 | 46.0 | 21.2
| HCB | 3.6 | 32.8 | 63.5
| JPT | 5.3 | 31.0 | 63.7
| YRI | 10.9 | 44.2 | 44.9
| ASW | 14.0 | 54.4 | 31.6
| CHB | 3.6 | 32.8 | 63.5
| CHD | 3.7 | 31.2 | 65.1
| GIH | 10.9 | 43.6 | 45.5
| LWK | 16.4 | 36.4 | 47.3
| MEX | 12.1 | 46.6 | 41.4
| MKK | 19.9 | 46.8 | 33.3
| TSI | 23.5 | 56.9 | 19.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=21187935
|Title=Genes Involved in the Metabolism of Poly-Unsaturated Fatty-Acids (PUFA) and Risk for Crohn's Disease in Children &amp; Young Adults
|OA=1
}}

{{PMID Auto
|PMID=21904596
|Title=Genetic Variation of the Human ?-2-Heremans-Schmid Glycoprotein (AHSG) Gene Associated with the Risk of SARS-CoV Infection
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}