List of variants in gene SCN8A reported as likely benign for Early Infantile Epileptic Encephalopathy, Autosomal Dominant

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.*3706del	rs560775301	0.00338
NM_001330260.2(SCN8A):c.2235_2236del	rs556349961	0.00093
NM_001330260.2(SCN8A):c.3914_3917dup	rs370929972
NM_001330260.2(SCN8A):c.5943GAG[1] (p.Ter1981=)	rs555793953

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