rs613872(G;T)

~5 fold higher risk for Fuchs' dystrophy, a corneal disorder

Magnitude
2.5Worth knowing
Repute
Bad
Frequency
11%Average of 9 populations
On SNPedia
rs613872(G;T)
Gene
TCF4

Frequency

Share of people with G;T in each HapMap population.

  • Tuscan30%
  • European ancestry (Utah)27%
  • Gujarati Indian17%
  • African ancestry (Southwest US)12%
  • Mexican ancestry (Los Angeles)12%
  • Maasai (Kenya)2%
  • Han Chinese (Beijing)2%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs613872

  1. G;GMost notableBad~20-30x higher risk for Fuchs' dystrophy, a corneal disorderWorth knowing · 2.52% of people
  2. T;TGoodcommon in complete genomicsTypical · 0.087% of people

All about rs613872

Source and license

Adapted from rs613872(G;T) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.