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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC102724058, SCN1A
Single nucleotide variant
(intron variant)
Severe myoclonic epilepsy in infancy
GLikely pathogenic
SCN1A
(G77R +5 more)
Single nucleotide variant
(missense variant +1 more)
Generalized epilepsy with febrile seizures plus, type 2
GLikely pathogenic
SCN1A
(C336R)
Single nucleotide variant
(missense variant +2 more)
Severe myoclonic epilepsy in infancy
GLikely pathogenic
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