rs3733591

A SNP in the SLC2A9 gene on chromosome 4. Its most notable genotype is C;C: common in clinvar

Gene
SLC2A9
Location
Chr 49,920,506 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
29%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. C;CMost notableGoodcommon in clinvarTypical · 0.053% of people

SNPedia records rs3733591 on the minus strand: (G;G). 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.

  • AverageC;C 53%
  • European ancestry (Utah)C;C 65%
  • Han Chinese (Beijing)C;C 7%
  • Japanese (Tokyo)C;C 9%
  • Yoruba (Nigeria)C;C 92%
  • African ancestry (Southwest US)C;C 84%
  • Chinese (Denver)C;C 17%
  • Gujarati IndianC;C 30%
  • Luhya (Kenya)C;C 89%
  • Mexican ancestry (Los Angeles)C;C 56%
  • Maasai (Kenya)C;C 80%
  • TuscanC;C 55%

Other SLC2A9 SNPs

All SLC2A9 SNPs

Notes

From SNPedia

Notes

Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.

Source and license

Adapted from rs3733591 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.