List of variants in gene combination LOC102724058, SCN1A reported as not provided 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.5870A>G (p.Glu1957Gly)	rs121918802	0.00016
NM_001165963.4(SCN1A):c.4907G>A (p.Arg1636Gln)	rs121917995

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