C4551804[trait identifier] AND "deCODE genetics, Amgen"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2574113	NM_000335.5(SCN5A):c.3388-1G>C	SCN5A	Single nucleotide variant (splice acceptor variant)	Brugada syndrome 1 +1 more	GLikely pathogenic
Select item 2574114	NM_000335.5(SCN5A):c.504C>A (p.Tyr168Ter)	SCN5A (Y168*)	Single nucleotide variant (nonsense +1 more)	Brugada syndrome 1 +1 more	GLikely pathogenic