List of variants in gene GH-LCR, SCN4A studied for Hypokalemic periodic paralysis, type 1

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.4937C>A (p.Thr1646Asn)	rs1345007864	0.00001
NM_000334.4(SCN4A):c.3404G>A (p.Arg1135His)	rs527236150
NM_000334.4(SCN4A):c.4342C>T (p.Arg1448Cys)	rs121908544
NM_000334.4(SCN4A):c.4352G>A (p.Arg1451His)	rs748517635

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