List of variants in gene SCN3A reported as likely benign for developmental and epileptic encephalopathy

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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_006922.4(SCN3A):c.3250G>A (p.Val1084Ile)	rs140990288	0.00518
NM_006922.4(SCN3A):c.171T>C (p.Ala57=)	rs111389453	0.00278
NM_006922.4(SCN3A):c.5232A>G (p.Pro1744=)	rs144587694	0.00035
NM_006922.4(SCN3A):c.2392-9A>G	rs199781617	0.00001

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