List of variants in gene SCN10A reported 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
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.4866T>C (p.Ser1622=)	rs6599242	0.93109
NM_006514.4(SCN10A):c.1476C>T (p.Leu492=)	rs7617919	0.20158
NM_006514.4(SCN10A):c.1284G>A (p.Glu428=)	rs62244070	0.20052
NM_006514.4(SCN10A):c.5217C>T (p.Asp1739=)	rs116353929	0.02232
NM_006514.4(SCN10A):c.4831G>A (p.Gly1611Arg)	rs777980971	0.00007
NM_006514.4(SCN10A):c.1534C>G (p.Arg512Gly)	rs200714519
NM_006514.4(SCN10A):c.5137= (p.Met1713=)	rs6599241
NM_006514.4(SCN10A):c.5140G>A (p.Val1714Ile)	rs1553612991

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