List of variants in gene combination GH-LCR, SCN4A reported as likely benign for Potassium-aggravated myotonia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.1677_1678insAT	rs397797581	0.01652
NM_000334.4(SCN4A):c.2717G>C (p.Ser906Thr)	rs41280102	0.01003
NM_000334.4(SCN4A):c.2341G>A (p.Val781Ile)	rs62070884	0.00873
NM_000334.4(SCN4A):c.2697G>A (p.Leu899=)	rs199827271	0.00044
NM_000334.4(SCN4A):c.4891G>A (p.Ala1631Thr)	rs201115695	0.00014
NM_000334.4(SCN4A):c.4083C>A (p.Ile1361=)	rs374480468	0.00011
NM_000334.4(SCN4A):c.4644C>T (p.Ser1548=)	rs751973449	0.00010
NM_000334.4(SCN4A):c.5401G>A (p.Ala1801Thr)	rs201192904	0.00010
NM_000334.4(SCN4A):c.3136G>T (p.Gly1046Trp)	rs759982229	0.00009
NM_000334.4(SCN4A):c.4282A>G (p.Ile1428Val)	rs368822028	0.00009
NM_000334.4(SCN4A):c.2256C>T (p.Leu752=)	rs375596512	0.00004
NM_000334.4(SCN4A):c.4289-4G>A	rs750364111	0.00004
NM_000334.4(SCN4A):c.5205G>C (p.Gln1735His)	rs199944673	0.00004
NM_000334.4(SCN4A):c.*670T>G	rs148552329	0.00003
NM_000334.4(SCN4A):c.2778C>T (p.Ile926=)	rs769634298	0.00002
NM_000334.4(SCN4A):c.4052C>T (p.Thr1351Met)	rs545724550	0.00002
NM_000334.4(SCN4A):c.3019G>A (p.Val1007Met)	rs781028684	0.00001
NM_000334.4(SCN4A):c.3604G>A (p.Glu1202Lys)	rs201916531	0.00001
NM_000334.4(SCN4A):c.4667A>G (p.Asn1556Ser)	rs751454852	0.00001
NM_000334.4(SCN4A):c.4709A>G (p.Asn1570Ser)	rs531658524	0.00001
NM_000334.4(SCN4A):c.2593G>C (p.Gly865Arg)	rs752159625
NM_000334.4(SCN4A):c.3062G>A (p.Arg1021His)	rs770497876
NM_000334.4(SCN4A):c.4222C>A (p.Arg1408Ser)	rs118047588

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