{{Rsnum
|rsid=3212183
|Gene=HNF4A
|Chromosome=20
|position=44406498
|Orientation=plus
|GMAF=0.3223
|Gene_s=HNF4A,MIR3646
|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 | 16.8 | 53.1 | 30.1
| HCB | 0.0 | 9.5 | 90.5
| JPT | 0.0 | 11.5 | 88.5
| YRI | 22.4 | 42.2 | 35.4
| ASW | 12.3 | 50.9 | 36.8
| CHB | 0.0 | 9.5 | 90.5
| CHD | 0.0 | 9.2 | 90.8
| GIH | 2.0 | 41.6 | 56.4
| LWK | 11.9 | 61.5 | 26.6
| MEX | 12.1 | 58.6 | 29.3
| MKK | 11.5 | 45.5 | 42.9
| TSI | 18.6 | 44.1 | 37.3
| HapMapRevision=28
}}
{{PMID Auto
|PMID=19748811
|Title=Influence of hepatocyte nuclear factor 4alpha (HNF4alpha) gene variants on the risk of type 2 diabetes: A meta-analysis in 49,577 individuals
}}

{{PMID Auto
|PMID=16186411
|Title=Variants in hepatocyte nuclear factor 4alpha are modestly associated with type 2 diabetes in Pima Indians.
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}