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From SNPedia

Magnitude 3
Repute Bad
Summary One or more G6PD deficiency-associated mutations detected in uploaded data.
Criteria Gs307/criteria

This genoset is expected to be observed primarily in females who are carriers of one (or possibly more) genotypes containing a class I, II or III (pathogenic) G6PD deficiency-associated mutation. Sons have a 50% chance of being G6PD deficient. Due to the random nature of X-chromosome inactivation, these (heterozygous) females may or may not have any G6PD deficiency themselves; only enzymatic testing for G6PD can determine that.

The genotype containing the specific mutation observed is listed separately in the individual's Promethease report.