List of variants in gene SCN2A reported as not provided for electroclinical syndrome

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.4565G>C (p.Gly1522Ala)	rs147522594	0.00016
NM_001040142.2(SCN2A):c.208C>G (p.Pro70Ala)
NM_001040142.2(SCN2A):c.2767T>C (p.Trp923Arg)	rs1057524573
NM_001040142.2(SCN2A):c.3671_3674dup (p.Ala1226fs)
NM_001040142.2(SCN2A):c.4264A>G (p.Lys1422Glu)	rs796053137
NM_001040142.2(SCN2A):c.4801G>T (p.Val1601Leu)	rs1553463140
NM_001040142.2(SCN2A):c.5272A>C (p.Ser1758Arg)	rs1064794005
NM_001040142.2(SCN2A):c.593T>A (p.Val198Asp)	rs1697272829

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