rs11465770(C;T)

Possibly lower risk of Crohn's Disease (OR=0.30)

Magnitude
1.5Minor
Repute
Not rated
Frequency
7%Average of 10 populations
On SNPedia
rs11465770(C;T)
Gene
IL23R

Frequency

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

  • Tuscan20%
  • Gujarati Indian18%
  • European ancestry (Utah)15%
  • African ancestry (Southwest US)5%
  • Mexican ancestry (Los Angeles)5%
  • Maasai (Kenya)5%
  • Luhya (Kenya)<1%
  • Han Chinese (Beijing)<1%
  • Yoruba (Nigeria)<1%
  • Japanese (Tokyo)0%

Other genotypes of rs11465770

  1. C;CNot ratednormal Crohn's Disease riskTypical · 0.093% of people
  2. T;TNot ratedpossibly lower risk of Crohn's Disease (OR=0.30)Minor · 1.5<1% of people

All about rs11465770

Source and license

Adapted from rs11465770(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.