{{Rsnum
|rsid=7202116
|Gene=FTO
|Chromosome=16
|position=53787703
|Orientation=plus
|GMAF=0.3549
|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 | 26.5 | 55.8 | 17.7
| HCB | 74.1 | 23.0 | 3.0
| JPT | 65.5 | 31.9 | 2.7
| YRI | 24.7 | 52.1 | 23.3
| ASW | 26.3 | 49.1 | 24.6
| CHB | 74.1 | 23.0 | 3.0
| CHD | 72.2 | 25.0 | 2.8
| GIH | 56.4 | 36.6 | 6.9
| LWK | 19.3 | 47.7 | 33.0
| MEX | 60.3 | 36.2 | 3.4
| MKK | 21.2 | 53.2 | 25.6
| TSI | 33.3 | 43.1 | 23.5
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22982992
  |Trait=Body mass index
  |Title=FTO genotype is associated with phenotypic variability of body mass index.
  |RiskAllele=G
  |Pval=2E-10
  |OR=.04
  |ORtxt=[0.025-0.047] unit increase
  |OA=1
}}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}