{{Rsnum
|rsid=2397084
|Gene=IL17F
|Chromosome=6
|position=52237046
|Orientation=plus
|GMAF=0.0404
|Gene_s=IL17F
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 0.9 | 9.7 | 89.4
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 0.0 | 100.0
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 2.8 | 97.2
| GIH | 0.0 | 11.9 | 88.1
| LWK | 0.0 | 2.7 | 97.3
| MEX | 0.0 | 15.8 | 84.2
| MKK | 0.0 | 1.9 | 98.1
| TSI | 0.0 | 18.8 | 81.2
| HapMapRevision=28
}}{{PMID Auto
|PMID=23111159
|Title=Genetic association between IL-17F gene polymorphisms and the pathogenesis of Graves' Disease in the Han Chinese population
}}

{{PMID Auto
|PMID=20618772
|Title=Association between IL-17F gene polymorphisms and susceptibility to and severity of rheumatoid arthritis (RA).
}}

{{PMID Auto
|PMID=24935327
|Title=Haplotype Analysis on Chromosome 6p of Tumor Necrosis Factor Alpha, Vascular Endothelial Growth Factor A, and Interleukin-17F Alleles Associated With Corneal Transplant Rejection
}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}