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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN2A
(V1601M)
Single nucleotide variant
(missense variant)
Seizures, benign familial infantile, 3
GLikely pathogenic
SCN2A
(F1986L)
Single nucleotide variant
(missense variant)
Seizures, benign familial infantile, 3
GUncertain significance
SCN2A
(D1999Y)
Single nucleotide variant
(missense variant)
Seizures, benign familial infantile, 3
GUncertain significance
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