rs17118154(C;C)

Common/normal

Magnitude
0.0Typical
Repute
Good
Frequency
96%Average of 4 populations
On SNPedia
rs17118154(C;C)
Gene
PMEL

Frequency

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

  • European ancestry (Utah)100%
  • Han Chinese (Beijing)100%
  • Japanese (Tokyo)100%
  • Yoruba (Nigeria)84%

Other genotypes of rs17118154

  1. C;GMost notableBadPossible mutation leading to pigment dispersion syndrome and pigmentary glaucomaVery important · 5.54% of people

All about rs17118154

Source and license

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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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