List of variants in gene SCN4A reported as likely benign for not specified

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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.366C>T (p.Arg122=)	rs41280108	0.04121
NM_000334.4(SCN4A):c.1167T>C (p.Tyr389=)	rs16947296	0.03818
NM_000334.4(SCN4A):c.355G>A (p.Val119Ile)	rs41280110	0.00232
NM_000334.4(SCN4A):c.612-18C>A	rs377510393	0.00232
NM_000334.4(SCN4A):c.1100+7G>A	rs200770684	0.00212
NM_000334.4(SCN4A):c.1453-4A>G	rs111818485	0.00209
NM_000334.4(SCN4A):c.218C>T (p.Pro73Leu)	rs75086141	0.00029
NM_000334.4(SCN4A):c.1653C>T (p.Cys551=)	rs201199086	0.00026
NM_000334.4(SCN4A):c.1935C>T (p.Phe645=)	rs181494727	0.00009
NM_000334.4(SCN4A):c.1710C>T (p.Ile570=)	rs760067411	0.00005
NM_000334.4(SCN4A):c.204C>T (p.Tyr68=)	rs80266947	0.00004
NM_000334.4(SCN4A):c.1593C>T (p.Ser531=)	rs139988178	0.00003
NM_000334.4(SCN4A):c.855G>A (p.Pro285=)	rs763725074	0.00003
NM_000334.4(SCN4A):c.969G>A (p.Thr323=)	rs1429424012	0.00002
NM_000334.4(SCN4A):c.703+6G>A	rs748828476	0.00001
NM_000334.4(SCN4A):c.1242+9del	rs1555604336
NM_000334.4(SCN4A):c.1452+8C>A	rs777701736
NM_000334.4(SCN4A):c.483-4C>G	rs200062384
NM_000334.4(SCN4A):c.483-9C>A	rs201552497

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