rs1114620

A SNP on chromosome 16. Its most notable genotype is T;T: common in complete genomics

Gene
None listed
Location
Chr 169,169,880 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe, FamilyTreeDNA
Minor allele frequency
13%

Genotypes

Plus strand, as in 23andMe and AncestryDNA files.

  1. T;TMost notableGoodcommon in complete genomicsTypical · 0.074% of people

SNPedia records rs1114620 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 74%
  • European ancestry (Utah)T;T 81%
  • Han Chinese (Beijing)T;T 80%
  • Japanese (Tokyo)T;T 71%
  • Yoruba (Nigeria)T;T 64%
  • African ancestry (Southwest US)T;T 67%
  • Chinese (Denver)T;T 73%
  • Gujarati IndianT;T 88%
  • Luhya (Kenya)T;T 66%
  • Mexican ancestry (Los Angeles)T;T 81%
  • Maasai (Kenya)T;T 74%
  • TuscanT;T 72%

Notes

From SNPedia

Notes

This SNP was (previously) easy to confuse with a different SNP, rs11146020, due to the similarity in the number and a current error in the OMIM database, which erroneously cites this SNP, rs1114620, in the first paragraph about Molecular Genetics on this webpage, where the correct citation for the Rice et al. paper should be to rs11146020.

Source and license

Adapted from rs1114620 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.