"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 48300	NM_000335.5(SCN5A):c.3360G>A (p.Ala1120=)	LOC110121269, SCN5A	Single nucleotide variant (synonymous variant +1 more)	Brugada syndrome +12 more	GConflicting classifications of pathogenicity
Select item 48298	NM_000335.5(SCN5A):c.3266C>T (p.Pro1089Leu)	LOC110121269, SCN5A (P1089L +1 more)	Single nucleotide variant (missense variant +1 more)	Dilated cardiomyopathy 1E +13 more	GBenign/Likely benign
Select item 9400	NM_000335.5(SCN5A):c.3157G>A (p.Glu1053Lys)	LOC110121269, SCN5A (E1053K)	Single nucleotide variant (missense variant)	Brugada syndrome +5 more	GConflicting classifications of pathogenicity
Select item 201486	NM_000335.5(SCN5A):c.2962C>T (p.Arg988Trp)	LOC110121269, SCN5A (R988W)	Single nucleotide variant (missense variant)	Cardiac arrhythmia +9 more	GUncertain significance
Select item 67769	NM_000335.5(SCN5A):c.2944T>C (p.Cys982Arg)	LOC110121269, SCN5A (C982R)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1E +12 more	GConflicting classifications of pathogenicity
Select item 48296	NM_000335.5(SCN5A):c.2788-6C>T	LOC110121269, SCN5A	Single nucleotide variant (intron variant)	Dilated cardiomyopathy 1E +9 more	GBenign/Likely benign

ClinVar