ClinVar Miner

List of variants in gene SCN1B reported as uncertain significance for Generalized epilepsy with febrile seizures plus, type 1; Brugada syndrome 5; Atrial fibrillation, familial, 13; Epileptic encephalopathy, early infantile, 52

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Total variants: 4
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HGVS dbSNP
NM_001037.5(SCN1B):c.134G>A (p.Arg45His) rs180943300
NM_001037.5(SCN1B):c.158C>A (p.Thr53Asn) rs1568348711
NM_001037.5(SCN1B):c.347C>T (p.Ser116Leu) rs1555720743
NM_001037.5(SCN1B):c.38T>C (p.Leu13Pro) rs786205834

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