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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SZT2
(V1063L)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 18
+1 more
GUncertain significance
SZT2
(R1882W +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 18
+2 more
GUncertain significance