{{Rsnum
|rsid=16953002
|Gene=FTO
|Chromosome=16
|position=54080912
|Orientation=plus
|GMAF=0.2057
|Gene_s=FTO
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 1.8 | 24.8 | 73.5
| HCB | 10.9 | 46.7 | 42.3
| JPT | 6.2 | 40.7 | 53.1
| YRI | 4.8 | 28.6 | 66.7
| ASW | 7.0 | 36.8 | 56.1
| CHB | 10.9 | 46.7 | 42.3
| CHD | 11.0 | 46.8 | 42.2
| GIH | 5.0 | 29.7 | 65.3
| LWK | 0.0 | 20.0 | 80.0
| MEX | 0.0 | 15.5 | 84.5
| MKK | 1.9 | 27.1 | 71.0
| TSI | 2.9 | 32.4 | 64.7
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23455637
  |Trait=Melanoma
  |Title=A variant in FTO shows association with melanoma risk not due to BMI.
  |RiskAllele=A
  |Pval=4E-12
  |OR=1.16
  |ORtxt=[1.11-1.20]
  |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}}