"Center for Medical Genetics Ghent, University of Ghent"[submitter] AN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 254159	NM_000218.3(KCNQ1):c.349C>T (p.Pro117Ser)	KCNQ1 (P117S)	Single nucleotide variant (missense variant)	Long QT syndrome 1	GLikely pathogenic
Select item 53086	NM_000218.3(KCNQ1):c.691C>T (p.Arg231Cys)	KCNQ1 (R231C +2 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GPathogenic/Likely pathogenic