rs1992662(A;A)

0.76x decreased risk for Crohn's disease

Magnitude
0.0Typical
Repute
Not rated
Frequency
32%Average of 4 populations
On SNPedia
rs1992662(T;T)Minus strand
Gene
PTGER4

Frequency

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

  • Yoruba (Nigeria)60%
  • European ancestry (Utah)45%
  • Han Chinese (Beijing)16%
  • Japanese (Tokyo)7%

Other genotypes of rs1992662

  1. G;GMost notableNot ratedincreased risk for Crohn's diseaseTypical · 0.034% of people
  2. A;GNot rated?Typical · 0.034% of people

All about rs1992662

Source and license

Adapted from rs1992662(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.