rs1452093

A SNP on chromosome 21. Its most notable genotype is A;G: common in complete genomics

Gene
None listed
Location
Chr 2127,372,037 (GRCh38)
Highest magnitude
0.0Typical
Tested on
AncestryDNA
Minor allele frequency
37%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. A;GMost notableGoodcommon in complete genomicsTypical · 0.039% of people

SNPedia records rs1452093 on the minus strand: (C;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.

  • AverageA;G 39%
  • European ancestry (Utah)A;G 47%
  • Han Chinese (Beijing)A;G 24%
  • Japanese (Tokyo)A;G 25%
  • Yoruba (Nigeria)A;G 22%
  • African ancestry (Southwest US)A;G 42%
  • Chinese (Denver)A;G 23%
  • Gujarati IndianA;G 55%
  • Luhya (Kenya)A;G 38%
  • Mexican ancestry (Los Angeles)A;G 60%
  • Maasai (Kenya)A;G 42%
  • TuscanA;G 52%

Source and license

Adapted from rs1452093 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.