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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PNPO
(E50K)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
PNPO
(K60*)
Single nucleotide variant
(nonsense)
Pyridoxal phosphate-responsive seizures
GPathogenic
PNPO
(R229Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PNPO
(R233Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GUncertain significance
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