List of variants in gene combination GH-LCR, SCN4A reported as not provided for Hyperkalemic periodic paralysis

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: 12

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HGVS	dbSNP	gnomAD frequency
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.2023C>T (p.Arg675Trp)	rs121908556	0.00001
NM_000334.4(SCN4A):c.2024G>A (p.Arg675Gln)	rs121908557	0.00001
NM_000334.4(SCN4A):c.2023C>G (p.Arg675Gly)	rs121908556
NM_000334.4(SCN4A):c.2065C>A (p.Leu689Ile)	rs80338955
NM_000334.4(SCN4A):c.4108A>G (p.Met1370Val)	rs80338960
NM_000334.4(SCN4A):c.4342C>A (p.Arg1448Ser)	rs121908544
NM_000334.4(SCN4A):c.4342C>T (p.Arg1448Cys)	rs121908544
NM_000334.4(SCN4A):c.4343G>A (p.Arg1448His)	rs121908545
NM_000334.4(SCN4A):c.4343G>C (p.Arg1448Pro)	rs121908545
NM_000334.4(SCN4A):c.4774A>G (p.Met1592Val)	rs80338962

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