rs11090865(G;T)

Carrier of a deafness-related modifier variant

Magnitude
2.3Worth knowing
Repute
Bad
Frequency
14%Average of 4 populations
On SNPedia
rs11090865(G;T)
Gene
TRMU

Frequency

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

  • European ancestry (Utah)31%
  • Yoruba (Nigeria)24%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%

Other genotypes of rs11090865

  1. G;GGoodcommon in clinvarTypical · 0.084% of people
  2. T;TMost notableBadModifier variant; some impact in rare casesImportant · 3.02% of people

All about rs11090865

Notes

From SNPedia

See text of main rs-page

Source and license

Adapted from rs11090865(G;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.