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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
G6PD
(A335T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GPathogenic
G6PD
(E317K +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
G6PD
(V68M +1 more)
Single nucleotide variant
(missense variant)
not specified
+5 more
GPathogenic/Likely pathogenic
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