List of variants in gene SCN8A reported as benign 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.4796-38C>A	rs303828	0.86075
NM_001330260.2(SCN8A):c.576C>T (p.Asp192=)	rs4761829	0.81114
NM_001330260.2(SCN8A):c.1135-48C>T	rs2291265	0.78368
NM_001330260.2(SCN8A):c.3490+20G>A	rs303808	0.76481
NM_001330260.2(SCN8A):c.4509T>C (p.Pro1503=)	rs303815	0.62374
NM_001330260.2(SCN8A):c.1833G>T (p.Arg611=)	rs35242963	0.01438
NM_001330260.2(SCN8A):c.2371-32A>C	rs303767
NM_001330260.2(SCN8A):c.2545-7dup	rs56879517
NM_001330260.2(SCN8A):c.5472C>A (p.Pro1824=)	rs60637

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