"MGZ Medical Genetics Center"[submitter] AND "SCN10A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 532077	NM_006514.4(SCN10A):c.4777A>T (p.Ile1593Phe)	SCN10A (I1593F +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +2 more	GUncertain significance
Select item 420025	NM_006514.4(SCN10A):c.2441G>A (p.Arg814His)	SCN10A (R814H +1 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2 +4 more	GConflicting classifications of pathogenicity
Select item 463239	NM_006514.4(SCN10A):c.2428G>T (p.Gly810Trp)	SCN10A (G810W +1 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2 +3 more	GConflicting classifications of pathogenicity
Select item 1709004	NM_006514.4(SCN10A):c.2246A>G (p.Lys749Arg)	SCN10A (K651R +1 more)	Single nucleotide variant (missense variant)	Episodic pain syndrome, familial, 2	GUncertain significance
Select item 463232	NM_006514.4(SCN10A):c.1370A>G (p.Glu457Gly)	SCN10A (E457G)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 1345265	NM_006514.4(SCN10A):c.644G>A (p.Arg215Gln)	SCN10A (R215Q)	Single nucleotide variant (missense variant)	Brugada syndrome +1 more	GUncertain significance
Select item 463260	NM_006514.4(SCN10A):c.472T>G (p.Tyr158Asp)	SCN10A (Y158D)	Single nucleotide variant (missense variant)	Brugada syndrome 1 +4 more	GConflicting classifications of pathogenicity

ClinVar