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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN2A
(R102*)
Single nucleotide variant
(nonsense)
not provided
+3 more
GPathogenic
SCN2A
(A176P)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 11
GUncertain significance
SCN2A
(V261M)
Single nucleotide variant
(missense variant)
Seizures, benign familial infantile, 3
+2 more
GPathogenic
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