ClinVar Miner

List of variants reported as likely benign for Migraine, familial hemiplegic, 3; Severe myoclonic epilepsy in infancy; Generalized epilepsy with febrile seizures plus, type 2; Developmental and epileptic encephalopathy 6B by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.3705+12T>G	rs147032678	0.00181
NM_001165963.4(SCN1A):c.2415+9A>G	rs2105827142
NM_001165963.4(SCN1A):c.602+6_602+7dup	rs577627288

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