List of variants in gene SCN2A reported as benign by PreventionGenetics, part of Exact Sciences

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.1035-3T>C	rs2121371	0.82016
NM_001040142.2(SCN2A):c.1672-16C>T	rs1867864	0.56164
NM_001040142.2(SCN2A):c.4914T>A (p.Arg1638=)	rs2060198	0.25169
NM_001040142.2(SCN2A):c.56G>A (p.Arg19Lys)	rs17183814	0.06063
NM_001040142.2(SCN2A):c.1785T>C (p.Asp595=)	rs141815642	0.01027
NM_001040142.2(SCN2A):c.5919C>T (p.Pro1973=)	rs73025979	0.00908
NM_001040142.2(SCN2A):c.5326C>T (p.Leu1776=)	rs138123155	0.00559
NM_001040142.2(SCN2A):c.2723A>G (p.Lys908Arg)	rs2228980	0.00365
NM_001040142.2(SCN2A):c.387-10G>A	rs2304015	0.00277
NM_001040142.2(SCN2A):c.3453C>T (p.Pro1151=)	rs145662546	0.00166
NM_001040142.2(SCN2A):c.5229A>G (p.Lys1743=)	rs2227898	0.00144
NM_001040142.2(SCN2A):c.100G>A (p.Ala34Thr)	rs144814658	0.00063

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