List of variants in gene SCN1B studied for electroclinical syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001037.5(SCN1B):c.472G>C (p.Val158Leu)	rs138450474	0.00002
NM_001037.5(SCN1B):c.388G>A (p.Glu130Lys)	rs1351632820	0.00001
NM_001037.5(SCN1B):c.85G>A (p.Glu29Lys)	rs767384862	0.00001

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