rs2286812(C;T)

~2x higher risk for Fuchs' dystrophy, a corneal disorder

Magnitude
1.5Minor
Repute
Bad
Frequency
18%Average of 10 populations
On SNPedia
rs2286812(C;T)
Gene
RPL12P10

Frequency

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

  • Gujarati Indian40%
  • Japanese (Tokyo)25%
  • Han Chinese (Beijing)24%
  • Mexican ancestry (Los Angeles)21%
  • European ancestry (Utah)18%
  • Chinese (Denver)16%
  • African ancestry (Southwest US)9%
  • Luhya (Kenya)8%
  • Maasai (Kenya)8%
  • Yoruba (Nigeria)6%

Other genotypes of rs2286812

  1. C;CGoodcommonTypical · 0.081% of people
  2. T;TMost notableBad~4x higher risk for Fuchs' dystrophy, a corneal disorderWorth knowing · 2.01% of people

All about rs2286812

Source and license

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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