List of variants in gene combination LOC110121269, SCN5A reported as uncertain significance by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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.3305C>A (p.Ser1102Tyr)	rs7626962	0.02208
NM_000335.5(SCN5A):c.2944T>C (p.Cys982Arg)	rs199473182	0.00033
NM_000335.5(SCN5A):c.2989G>A (p.Ala997Thr)	rs137854609	0.00008
NM_000335.5(SCN5A):c.2956C>T (p.Arg986Trp)	rs561547165	0.00004
NM_000335.5(SCN5A):c.3080G>A (p.Arg1027Gln)	rs763891399	0.00004
NM_000335.5(SCN5A):c.2819G>A (p.Ser940Asn)	rs879123756	0.00001

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