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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
G6PD
(S188F +1 more)
Single nucleotide variant
(missense variant)
not provided
+7 more
GPathogenic/Likely pathogenic
G6PD
(N126D +1 more)
Single nucleotide variant
(missense variant)
G6PD deficiency
+4 more
GConflicting classifications of pathogenicity
G6PD
(V68M +1 more)
Single nucleotide variant
(missense variant)
G6PD deficiency
+5 more
GPathogenic/Likely pathogenic
G6PD
(I48T +1 more)
Single nucleotide variant
(missense variant)
Anemia, nonspherocytic hemolytic, due to G6PD deficiency
+3 more
GPathogenic/Likely pathogenic
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