List of variants in gene SCN10A reported by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006514.4(SCN10A):c.3803G>A (p.Arg1268Gln)	rs138832868	0.00259
NM_006514.4(SCN10A):c.2441G>A (p.Arg814His)	rs139861061	0.00041
NM_006514.4(SCN10A):c.2428G>T (p.Gly810Trp)	rs145712124	0.00030
NM_006514.4(SCN10A):c.365C>T (p.Thr122Met)	rs142884499	0.00016
NM_006514.4(SCN10A):c.243T>A (p.Asp81Glu)	rs1060501717

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