rs2066844(T;T)

Significance unclear; possibly higher risk for Crohn's disease

Magnitude
3.1Important
Repute
Bad
Frequency
0%Average of 10 populations
On SNPedia
rs2066844(T;T)
Gene
NOD2

Frequency

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

  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%
  • Yoruba (Nigeria)0%
  • African ancestry (Southwest US)0%
  • Chinese (Denver)0%
  • Luhya (Kenya)0%
  • Mexican ancestry (Los Angeles)0%
  • Maasai (Kenya)0%
  • Tuscan0%

Other genotypes of rs2066844

  1. C;CGoodcommon in complete genomicsTypical · 0.096% of people
  2. C;TBadSignificance is unclear, but possibly, ~2x higher risk for Crohn's diseaseWorth knowing · 2.04% of people

All about rs2066844

Source and license

Adapted from rs2066844(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.