{{Rsnum
|rsid=3781907
|Gene=UCP3
|Chromosome=11
|position=74005424
|Orientation=minus
|GMAF=0.2966
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=UCP3
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 7.1 | 46.0 | 46.9
| HCB | 18.2 | 53.3 | 28.5
| JPT | 16.8 | 43.4 | 39.8
| YRI | 7.5 | 34.7 | 57.8
| ASW | 8.8 | 31.6 | 59.6
| CHB | 18.2 | 53.3 | 28.5
| CHD | 22.2 | 48.1 | 29.6
| GIH | 5.0 | 30.7 | 64.4
| LWK | 2.7 | 34.5 | 62.7
| MEX | 8.6 | 25.9 | 65.5
| MKK | 1.3 | 21.8 | 76.9
| TSI | 5.9 | 35.3 | 58.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=19769793
|Title=Variation in the UCP2 and UCP3 genes associates with abdominal obesity and serum lipids: The Finnish Diabetes Prevention Study
|OA=1
}}

{{PMID Auto
|PMID=24124336
|Title=Association between UCP3 gene polymorphisms and nonalcoholic fatty liver disease in Chinese children
|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}}