List of variants in gene SCN4A reported as likely pathogenic for Hyperkalemic periodic paralysis

Minimum submission review status:		Collection method:
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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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000334.4(SCN4A):c.2005C>T (p.Arg669Cys)	rs897448432	0.00001
NM_000334.4(SCN4A):c.665G>A (p.Arg222Gln)	rs865887222	0.00001
NM_000334.4(SCN4A):c.1037-1G>A
NM_000334.4(SCN4A):c.1333G>T (p.Val445Leu)	rs121908552
NM_000334.4(SCN4A):c.1606+1G>C
NM_000334.4(SCN4A):c.1762A>G (p.Ile588Val)	rs2144798704
NM_000334.4(SCN4A):c.2012T>G (p.Phe671Cys)	rs772873287
NM_000334.4(SCN4A):c.611+1G>A
NM_000334.4(SCN4A):c.715A>G (p.Ile239Val)	rs1909519361
NM_000334.4(SCN4A):c.749T>G (p.Leu250Arg)	rs1057521065

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