List of variants in gene SCN5A reported as likely pathogenic by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.3908C>T (p.Thr1303Met)	rs199473603	0.00021
NM_000335.5(SCN5A):c.3715G>C (p.Glu1239Gln)	rs199473211	0.00003
NM_000335.5(SCN5A):c.4219G>A (p.Gly1407Arg)	rs137854612

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