rs2224721

A SNP in the HTR2A gene on chromosome 13. Its most notable genotype is G;G: common/normal

Gene
HTR2A
Location
Chr 1346,858,019 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA, FamilyTreeDNA
Minor allele frequency
32%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. G;GMost notableGoodcommon/normalTypical · 0.040% of people

SNPedia records rs2224721 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 4 HapMap populations.

  • AverageG;G 40%
  • European ancestry (Utah)G;G 50%
  • Han Chinese (Beijing)G;G 53%
  • Japanese (Tokyo)G;G 30%
  • Yoruba (Nigeria)G;G 26%

Conditions, medicines and genes

Notes

From SNPedia

Notes

: "Haplotype association analysis suggests that the haplotype CCGCA (at SNPs rs3125, rs6314, rs1923886, rs2224721 and rs2770296) is protective against bipolar disorder (P = 0.021, odds ratio 0.63) and the rarer haplotype CCACG confers risk to the disorder (P = 0.0065, odds ratio 3.08)."

Source and license

Adapted from rs2224721 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.