rs3751812

A SNP in the FTO gene on chromosome 16. Its most notable genotype is G;G: normal

Gene
FTO
Location
Chr 1653,784,548 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
24%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. G;GMost notableNot ratednormalTypical · 0.066% of people
  2. G;TNot ratedNo summary available.Typical · 0.028% of people
  3. T;TNot ratedincreased risk of obesityTypical · 0.05% of people

On SNPedia: (G;G), (G;T), (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.

  • AverageG;G 66% G;T 28% T;T 5%
  • European ancestry (Utah)G;G 27% G;T 56% T;T 18%
  • Han Chinese (Beijing)G;G 74% G;T 24% T;T 2%
  • Japanese (Tokyo)G;G 66% G;T 32% T;T 3%
  • Yoruba (Nigeria)G;G 88% G;T 12% T;T 0%
  • African ancestry (Southwest US)G;G 79% G;T 21% T;T 0%
  • Chinese (Denver)G;G 72% G;T 26% T;T 3%
  • Gujarati IndianG;G 56% G;T 37% T;T 7%
  • Luhya (Kenya)G;G 96% G;T 4% T;T 0%
  • Mexican ancestry (Los Angeles)G;G 66% G;T 33% T;T 2%
  • Maasai (Kenya)G;G 75% G;T 24% T;T <1%
  • TuscanG;G 33% G;T 43% T;T 24%

Notes

From SNPedia

Notes

Within the FTO gene, many SNPs appear to be co-inherited. The SNP showing the strongest association with body weight (i.e. body mass index, BMI) is not rs3751812, although this SNP is one of the co-inherited SNPs in the FTO gene region. For more information, refer to the FTO gene or the most studied FTO SNPs, rs9930506 or rs9939609. 23andMe considers rs3751812(T) equivalent to the rs9939609(A) implicated for african americans

Source and license

Adapted from rs3751812 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.