{{Rsnum
|rsid=1885088
|Gene=HNF4A
|Chromosome=20
|position=44410400
|Orientation=plus
|GMAF=0.09642
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=HNF4A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 3.5 | 33.6 | 62.8
| HCB | 0.0 | 0.7 | 99.3
| JPT | 0.0 | 0.9 | 99.1
| YRI | 0.0 | 2.0 | 98.0
| ASW | 0.0 | 3.5 | 96.5
| CHB | 0.0 | 0.7 | 99.3
| CHD | 0.0 | 2.8 | 97.2
| GIH | 0.0 | 19.8 | 80.2
| LWK | 0.0 | 1.8 | 98.2
| MEX | 6.9 | 32.8 | 60.3
| MKK | 0.0 | 14.8 | 85.2
| TSI | 4.9 | 27.5 | 67.6
| HapMapRevision=28
}}{{PMID Auto
|PMID=19406499
|Title=Interaction between HNF4A polymorphisms and physical activity in relation to type 2 diabetes-related traits: Results from the Quebec Family Study
}}

{{PMID Auto
|PMID=21633728
|Title=Hepatocyte nuclear factor 4 alpha P2 promoter variants associate with insulin resistance
}}

{{PMID Auto
|PMID=15735891
|Title=Variation near the hepatocyte nuclear factor (HNF)-4alpha gene associates with type 2 diabetes in the Danish population.
}}

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

{{PMID Auto
|PMID=16752173
|Title=Common variants in MODY genes increase the risk of gestational diabetes mellitus.
}}

{{PMID Auto
|PMID=18602983
|Title=Heterogeneity in gene loci associated with type 2 diabetes on human chromosome 20q13.1.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}