List of variants in gene SCN5A reported as pathogenic by Mayo Clinic Laboratories, Mayo Clinic

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.673C>T (p.Arg225Trp)	rs199473072	0.00008
NM_000335.5(SCN5A):c.4882C>T (p.Arg1628Ter)	rs199473284	0.00001
NM_000335.5(SCN5A):c.4928G>A (p.Arg1643His)	rs28937316	0.00001
NM_000335.5(SCN5A):c.1338+2T>A	rs786204839
NM_000335.5(SCN5A):c.1936del (p.Gln646fs)	rs727505158
NM_000335.5(SCN5A):c.4844TCT[1] (p.Phe1616del)	rs749697698

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