List of variants in gene SCN2A reported as pathogenic by Revvity Omics, Revvity

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001040142.2(SCN2A):c.1819C>T (p.Arg607Ter)	rs746060762
NM_001040142.2(SCN2A):c.4303C>T (p.Arg1435Ter)	rs796053138
NM_001040142.2(SCN2A):c.4446+1A>G	rs2105384790
NM_001040142.2(SCN2A):c.5644C>G (p.Arg1882Gly)	rs796053166

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