"Centre of Medical Genetics, University of Antwerp"[submitter] AND "SC - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 254157	NM_001160160.2(SCN5A):c.4714+95GGGT[3]	SCN5A	Microsatellite (intron variant)	not provided +1 more	GLikely pathogenic
Select item 830371	NM_000335.5(SCN5A):c.4708T>C (p.Phe1570Leu)	SCN5A (F1517L +4 more)	Single nucleotide variant (missense variant)	Brugada syndrome	GLikely pathogenic