| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Anemia, nonspherocytic hemolytic, due to G6PD deficiency +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Anemia, nonspherocytic hemolytic, due to G6PD deficiency +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Decreased glucose-6-phosphate dehydrogenase level in blood +8 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Malaria, susceptibility to +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Anemia, nonspherocytic hemolytic, due to G6PD deficiency +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
| | G6PD, IKBKG (H32R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +4 more | GPathogenic/Likely pathogenic |