List of variants in gene SCN5A reported as likely benign by Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.4215G>A (p.Gly1405=)	rs41311123	0.00859
NM_000335.5(SCN5A):c.5364C>T (p.Asp1788=)	rs375752426	0.00011
NM_000335.5(SCN5A):c.3388-7T>C	rs41310769	0.00009
NM_000335.5(SCN5A):c.1281C>T (p.Thr427=)	rs375989197	0.00004
NM_000335.5(SCN5A):c.2667C>T (p.Leu889=)	rs587781162	0.00002
NM_000335.5(SCN5A):c.5772C>G (p.Ser1924=)	rs199687668	0.00001
NM_000335.5(SCN5A):c.6000C>T (p.Leu2000=)	rs538707712	0.00001
NM_000335.5(SCN5A):c.4296+9C>A	rs572950088

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