List of variants in gene SCN5A reported as uncertain significance for Long QT syndrome 3; Brugada syndrome

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: 4

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HGVS	dbSNP
NM_000335.4(SCN5A):c.2497G>A (p.Gly833Arg)	rs45475899
NM_000335.5(SCN5A):c.2770G>A (p.Val924Ile)	rs199473177
NM_198056.2(SCN5A):c.3425C>T (p.Ala1142Val)	rs879255356
NM_198056.2(SCN5A):c.3577C>T (p.Arg1193Trp)	rs192379242

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