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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN2A
(A880S)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 11
+2 more
GLikely pathogenic
SCN2A
(R1882G)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 11
+2 more
GPathogenic