ClinVar Miner

List of variants in gene SCN1A reported as benign for Familial hemiplegic migraine type 3; Severe myoclonic epilepsy in infancy; Generalized epilepsy with febrile seizures plus, type 2

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Total variants: 2
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HGVS dbSNP
NM_001165963.4(SCN1A):c.1212A>G (p.Val404=) rs7580482
NM_001165963.4(SCN1A):c.2947-41C>T rs7601520

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