rs1992660(C;T)

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Magnitude
0.0Typical
Repute
Not rated
Frequency
33%Average of 4 populations
On SNPedia
rs1992660(A;G)Minus strand
Gene
PTGER4

Frequency

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

  • European ancestry (Utah)52%
  • Yoruba (Nigeria)49%
  • Japanese (Tokyo)16%
  • Han Chinese (Beijing)16%

Other genotypes of rs1992660

  1. T;TMost notableBadincreased risk for Crohn's diseaseTypical · 0.021% of people
  2. C;CGood0.72x decreased risk for Crohn's diseaseTypical · 0.046% of people

All about rs1992660

Source and license

Adapted from rs1992660(A;G) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.