List of variants reported as likely benign for myoclonus, familial

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001330260.2(SCN8A):c.4122T>A (p.Thr1374=)	rs115623439	0.00531
NM_001330260.2(SCN8A):c.141C>T (p.Asp47=)	rs149013279	0.00196
NM_001330260.2(SCN8A):c.4278G>A (p.Arg1426=)	rs143867796	0.00183
NM_001330260.2(SCN8A):c.2098A>T (p.Ile700Leu)	rs187153231	0.00138

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