List of variants in gene SCN1B reported as likely pathogenic for genetic generalized epilepsy

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.363C>G (p.Cys121Trp)	rs104894718	0.00003
NM_001037.5(SCN1B):c.373C>T (p.Arg125Cys)	rs1135401736	0.00001
NM_001037.5(SCN1B):c.253C>T (p.Arg85Cys)	rs786205830
NM_001037.5(SCN1B):c.254G>T (p.Arg85Leu)

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