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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN1A
(N115K)
Single nucleotide variant
(missense variant +2 more)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GPathogenic
STX1B
(E96*)
Single nucleotide variant
(nonsense)
Generalized epilepsy with febrile seizures plus
GPathogenic