List of variants reported as uncertain significance for Severe myoclonic epilepsy in infancy by New York Genome Center

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001165963.4(SCN1A):c.2201G>A (p.Cys734Tyr)	rs1247949520	0.00003
NM_001165963.4(SCN1A):c.5978T>C (p.Ile1993Thr)	rs766656231	0.00002
NM_001165963.4(SCN1A):c.2044G>A (p.Gly682Arg)	rs1398374184

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