rs2069556

A SNP in the TG gene on chromosome 8. Its most notable genotype is A;A: common in clinvar

Gene
TG
Location
Chr 8132,908,273 (GRCh38)
Highest magnitude
0.0Typical
Tested on
23andMe
Minor allele frequency
42%

Genotypes

As shown in 23andMe and AncestryDNA files.

  1. A;AMost notableGoodcommon in clinvarTypical · 0.043% of people
  2. A;GNot ratedNo summary available.Typical · 0.039% of people

On SNPedia: (A;A), (A;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.

Frequency

Share of each genotype in 10 HapMap populations.

  • AverageA;A 43% A;G 39%
  • European ancestry (Utah)A;A 20% A;G 50%
  • Han Chinese (Beijing)A;A 40% A;G 52%
  • Japanese (Tokyo)A;A 41% A;G 50%
  • Yoruba (Nigeria)A;A 95% A;G 6%
  • Chinese (Denver)A;A 36% A;G 51%
  • Gujarati IndianA;A 18% A;G 52%
  • Luhya (Kenya)A;A 91% A;G 9%
  • Mexican ancestry (Los Angeles)A;A 7% A;G 51%
  • Maasai (Kenya)A;A 69% A;G 28%
  • TuscanA;A 17% A;G 45%

Other TG SNPs

All TG SNPs

Source and license

Adapted from rs2069556 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.