rs1050152(C;T)

2.1x increased risk of Crohn's disease

Magnitude
2.0Worth knowing
Repute
Bad
Frequency
18%Average of 10 populations
On SNPedia
rs1050152(C;T)
Gene
SLC22A4

Frequency

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

  • European ancestry (Utah)58%
  • Tuscan43%
  • Mexican ancestry (Los Angeles)38%
  • African ancestry (Southwest US)19%
  • Gujarati Indian19%
  • Maasai (Kenya)3%
  • Chinese (Denver)3%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%

Other genotypes of rs1050152

  1. C;CGoodnormalTypical · 0.078% of people
  2. T;TMost notableBad2.1x increased risk of Crohn's diseaseWorth knowing · 2.13% of people

All about rs1050152

Source and license

Adapted from rs1050152(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.