{{Rsnum
|rsid=745975
|Gene=HNF4A
|Chromosome=20
|position=44406053
|Orientation=minus
|GMAF=0.1896
|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 | 6.2 | 38.1 | 55.8
| HCB | 5.1 | 29.2 | 65.7
| JPT | 0.9 | 29.2 | 69.9
| YRI | 1.4 | 11.6 | 87.1
| ASW | 0.0 | 36.8 | 63.2
| CHB | 5.1 | 29.2 | 65.7
| CHD | 1.8 | 37.6 | 60.6
| GIH | 4.0 | 26.7 | 69.3
| LWK | 0.9 | 17.3 | 81.8
| MEX | 0.0 | 20.7 | 79.3
| MKK | 1.9 | 24.4 | 73.7
| TSI | 6.9 | 32.4 | 60.8
| 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=16883527
|Title=[Scanning the HNF4A gene mutation from Chinese pedigrees with early- and/or multiple-onset diabetes].
}}

{{PMID Auto
|PMID=18340007
|Title=Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.
|OA=1
}}

{{PMID Auto
|PMID=18728231
|Title=Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies.
|OA=1
}}

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