List of variants in gene SCN2B reported 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
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_004588.5(SCN2B):c.205T>C (p.Tyr69His)	rs369196654	0.00009
NM_004588.5(SCN2B):c.640G>A (p.Ala214Thr)	rs200264107	0.00008
NM_004588.5(SCN2B):c.82C>T (p.Arg28Trp)	rs17121819	0.00007
NM_004588.5(SCN2B):c.140G>A (p.Arg47His)	rs17121818	0.00006
NM_004588.5(SCN2B):c.478G>A (p.Val160Met)	rs774317271	0.00006
NM_004588.5(SCN2B):c.5A>G (p.His2Arg)	rs765743471	0.00006
NM_004588.5(SCN2B):c.629C>T (p.Pro210Leu)	rs144248214	0.00006
NM_004588.5(SCN2B):c.461G>A (p.Arg154Gln)	rs753389706	0.00004
NM_004588.5(SCN2B):c.295G>A (p.Val99Met)	rs772817742	0.00002
NM_004588.5(SCN2B):c.44C>T (p.Thr15Met)	rs201373014	0.00002
NM_004588.5(SCN2B):c.237G>C (p.Met79Ile)	rs142643516	0.00001
NM_004588.5(SCN2B):c.452C>A (p.Pro151His)	rs765701955
NM_004588.5(SCN2B):c.578C>G (p.Thr193Arg)	rs115353159

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