rs749052

A SNP on chromosome 2. Its most notable genotype is T;T: common on affy axiom data

Gene
None listed
Location
Chr 2231,931,900 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, AncestryDNA
Minor allele frequency
6%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon on affy axiom dataTypical · 0.088% of people

SNPedia records rs749052 on the minus strand: (A;A). 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 88%
  • European ancestry (Utah)T;T 85%
  • Han Chinese (Beijing)T;T 98%
  • Japanese (Tokyo)T;T 99%
  • Yoruba (Nigeria)T;T 71%
  • African ancestry (Southwest US)T;T 81%
  • Chinese (Denver)T;T 99%
  • Gujarati IndianT;T 88%
  • Luhya (Kenya)T;T 85%
  • Mexican ancestry (Los Angeles)T;T 98%
  • Maasai (Kenya)T;T 86%
  • TuscanT;T 78%

Notes

From SNPedia

Notes

Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. Assessing the impact of global versus local ancestry in association studies.

Source and license

Adapted from rs749052 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.