List of variants in gene combination LOC102724058, SCN1A reported as likely pathogenic for Migraine, familial hemiplegic, 3; Severe myoclonic epilepsy in infancy; Generalized epilepsy with febrile seizures plus, type 2; Developmental and epileptic encephalopathy 6B

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3734G>A (p.Arg1245Gln)	rs121917912	0.00001
NM_001165963.4(SCN1A):c.4322C>T (p.Ala1441Val)	rs2105486615
NM_001165963.4(SCN1A):c.5316del (p.Ser1773fs)

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