rs17118154(C;G)

Possible mutation leading to pigment dispersion syndrome and pigmentary glaucoma

Magnitude
5.5Very important
Repute
Bad
Frequency
4%Average of 4 populations
On SNPedia
rs17118154(C;G)
Gene
PMEL

Frequency

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

  • Yoruba (Nigeria)16%
  • European ancestry (Utah)0%
  • Han Chinese (Beijing)0%
  • Japanese (Tokyo)0%

Other genotypes of rs17118154

  1. C;CGoodcommon/normalTypical · 0.096% of people

All about rs17118154

Notes

From SNPedia

see text at main rs-page

Source and license

Adapted from rs17118154(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.