List of variants in gene SCN5A reported as not provided for Conduction system disorder

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.1535C>T (p.Thr512Ile)	rs199473118	0.00001
NM_000335.5(SCN5A):c.4892G>A (p.Arg1631His)	rs199473286	0.00001
NM_000335.5(SCN5A):c.689T>C (p.Ile230Thr)	rs199473073	0.00001
NM_000335.5(SCN5A):c.1540G>T (p.Gly514Cys)	rs137854606
NM_000335.5(SCN5A):c.4856C>A (p.Thr1619Lys)	rs199473282

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