List of variants in gene SCN2A reported by GenomeConnect, ClinGen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001040142.2(SCN2A):c.4565G>C (p.Gly1522Ala)	rs147522594	0.00016
NM_001040142.2(SCN2A):c.5752C>T (p.Arg1918Cys)	rs139899756	0.00010
NM_001040142.2(SCN2A):c.1511_1512del (p.Arg504fs)	rs2105259822
NM_001040142.2(SCN2A):c.1988T>A (p.Leu663His)	rs2467934487
NM_001040142.2(SCN2A):c.2960G>A (p.Ser987Asn)	rs796053124
NM_001040142.2(SCN2A):c.4591C>T (p.Gln1531Ter)	rs1553463032
NM_001040142.2(SCN2A):c.4727del (p.Gly1576fs)	rs1553463096
NM_001040142.2(SCN2A):c.4801G>T (p.Val1601Leu)	rs1553463140

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