rs137852329(C;G)

Carrier of G6PD deficiency mutation; variable expressivity

Magnitude
3.0Important
Repute
Bad
On SNPedia
rs137852329(C;G)Minus strand
Gene
G6PD

Other genotypes of rs137852329

  1. T;TMost notableBadG6PD deficiencyVery important · 5.0
  2. G;TBadCarrier of G6PD deficiency mutation; variable expressivityImportant · 3.0
  3. G;GGoodcommon in clinvarTypical · 0.0
  4. C;CBadG6PD deficiencyVery important · 5.0

All about rs137852329

Notes

From SNPedia

Carrier but likely to be asymptomatic. However, effects vary in females due to random X chromosome inactivation.

Source and license

Adapted from rs137852329(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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.