List of variants in gene SCN2A reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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.1712G>A (p.Arg571His)	rs138138150	0.00013
NM_001040142.2(SCN2A):c.1901T>C (p.Val634Ala)	rs756119996	0.00001
NM_001040142.2(SCN2A):c.3049G>C (p.Val1017Leu)	rs769267899	0.00001
NM_001040142.2(SCN2A):c.3190G>T (p.Asp1064Tyr)	rs769395683	0.00001
NM_001040142.2(SCN2A):c.106A>G (p.Arg36Gly)	rs796053167
NM_001040142.2(SCN2A):c.1385C>T (p.Ala462Val)	rs769825203
NM_001040142.2(SCN2A):c.1861C>T (p.Arg621Cys)	rs796053205
NM_001040142.2(SCN2A):c.2696G>A (p.Gly899Asp)	rs796053121
NM_001040142.2(SCN2A):c.3413C>G (p.Thr1138Ser)	rs2105355734
NM_001040142.2(SCN2A):c.3457G>A (p.Glu1153Lys)	rs200138205
NM_001040142.2(SCN2A):c.4246C>T (p.Leu1416Phe)	rs1559399522
NM_001040142.2(SCN2A):c.5278A>G (p.Ile1760Val)	rs1702022330

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