List of variants in gene SCN5A reported as uncertain significance by Genetics and Genomics Program, Sidra Medicine

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	gnomAD frequency
NM_000335.5(SCN5A):c.1336G>A (p.Glu446Lys)	rs199473339	0.00007
NM_000335.5(SCN5A):c.142G>A (p.Glu48Lys)	rs199473048	0.00006
NM_000335.5(SCN5A):c.2014G>A (p.Ala672Thr)	rs199473140	0.00002
NM_000335.5(SCN5A):c.1604G>A (p.Arg535Gln)	rs199473121	0.00001

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