"Pediatrics, MediClubGeorgia"[submitter] AND "SCN2A"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 808846	NM_001040142.2(SCN2A):c.2638G>T (p.Ala880Ser)	SCN2A (A880S)	Single nucleotide variant (missense variant)	Seizures, benign familial infantile, 3 +2 more	GLikely pathogenic
Select item 207028	NM_001040142.2(SCN2A):c.5644C>G (p.Arg1882Gly)	SCN2A (R1882G)	Single nucleotide variant (missense variant)	Seizures, benign familial infantile, 3 +2 more	GPathogenic