List of variants reported as uncertain significance for Migraine, familial hemiplegic, 3; Severe myoclonic epilepsy in infancy; Generalized epilepsy with febrile seizures plus, type 2; Developmental and epileptic encephalopathy 6B by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.5217C>T (p.Pro1739=)	rs149315236	0.00011
NM_001165963.4(SCN1A):c.1803C>T (p.Asn601=)	rs139403702	0.00006
NM_001165963.4(SCN1A):c.1343T>C (p.Ile448Thr)	rs755962326	0.00002
NM_001165963.4(SCN1A):c.5263G>A (p.Asp1755Asn)	rs927722314	0.00001

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