List of variants in gene SCN5A reported as likely 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.3905G>A (p.Arg1302Gln)	rs977717858	0.00004
NM_000335.5(SCN5A):c.1127G>A (p.Arg376His)	rs199473101	0.00003
NM_000335.5(SCN5A):c.1099C>T (p.Arg367Cys)	rs199473097	0.00001
NM_000335.5(SCN5A):c.5126C>T (p.Ser1709Leu)	rs137854604	0.00001
NM_000335.5(SCN5A):c.1058C>T (p.Thr353Ile)	rs199473096
NM_000335.5(SCN5A):c.5358_5361del (p.Ser1786fs)	rs1559720961

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