rs2286812(T;T)

~4x higher risk for Fuchs' dystrophy, a corneal disorder

Magnitude
2.0Worth knowing
Repute
Bad
Frequency
1%Average of 10 populations
On SNPedia
rs2286812(T;T)
Gene
RPL12P10

Frequency

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

  • Gujarati Indian3%
  • European ancestry (Utah)2%
  • Japanese (Tokyo)2%
  • African ancestry (Southwest US)2%
  • Mexican ancestry (Los Angeles)2%
  • Han Chinese (Beijing)2%
  • Chinese (Denver)1%
  • Yoruba (Nigeria)<1%
  • Luhya (Kenya)0%
  • Maasai (Kenya)0%

Other genotypes of rs2286812

  1. C;CGoodcommonTypical · 0.081% of people
  2. C;TBad~2x higher risk for Fuchs' dystrophy, a corneal disorderMinor · 1.518% of people

All about rs2286812

Source and license

Adapted from rs2286812(T;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.