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

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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: 3

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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.254G>A (p.Arg85His)	rs16969925	0.00002
NM_001037.5(SCN1B):c.208-2A>C	rs724159982

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