rs7204609

A SNP in the FTO gene on chromosome 16. Its most notable genotype is T;T: common in complete genomics

Gene
FTO
Location
Chr 1653,799,693 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA
Minor allele frequency
23%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.054% of people

On SNPedia: (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 11 HapMap populations.

  • AverageT;T 54%
  • European ancestry (Utah)T;T 97%
  • Han Chinese (Beijing)T;T 32%
  • Japanese (Tokyo)T;T 32%
  • Yoruba (Nigeria)T;T 33%
  • African ancestry (Southwest US)T;T 40%
  • Chinese (Denver)T;T 39%
  • Gujarati IndianT;T 85%
  • Luhya (Kenya)T;T 34%
  • Mexican ancestry (Los Angeles)T;T 74%
  • Maasai (Kenya)T;T 36%
  • TuscanT;T 95%

Notes

From SNPedia

Notes

Variations in the FTO gene are associated with severe obesity in the Japanese. FTO gene variation and measures of body mass in an African population. Analysis of FTO gene variants with measures of obesity and glucose homeostasis in the IRAS Family Study. Design and evaluation of a treatment programme for Spanish adolescents with overweight and obesity. The EVASYON Study. FTO genetic variation and association with obesity in West Africans and African Americans. A latent variable partial least squares path modeling approach to regional association and polygenic effect with applications to a human obesity study.

Source and license

Adapted from rs7204609 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.

SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.