List of variants in gene combination LOC110121288, 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.3218T>C (p.Val1073Ala)	rs6795970	0.70355
NM_006514.4(SCN10A):c.3275T>C (p.Leu1092Pro)	rs12632942	0.21722
NM_006514.4(SCN10A):c.3393C>G (p.Thr1131=)	rs6771157	0.21708
NM_006514.4(SCN10A):c.2884A>G (p.Ile962Val)	rs57326399	0.20797
NM_006514.4(SCN10A):c.2937C>T (p.Gly979=)	rs59468016	0.18899
NM_006514.4(SCN10A):c.3192G>A (p.Thr1064=)	rs6791171	0.15667

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