rs76723693(A;G)
Carrier of G6PD deficiency mutation; variable expressivity; Hb1Ac value may need adjusting for diabetes diagnosis
- Magnitude
- 3.0Important
- Repute
- Bad
- On SNPedia
- rs76723693(C;T)Minus strand
- Gene
- G6PD
Other genotypes of rs76723693
Notes
From SNPedia
Carrier but likely to be asymptomatic. However, effects vary in females due to random X chromosome inactivation.
Related
Source and license
Adapted from rs76723693(C;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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.