List of variants reported as likely pathogenic for long QT syndrome by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.2684C>T (p.Thr895Met)	rs199473434	0.00005
NM_000238.4(KCNH2):c.2863C>G (p.Leu955Val)	rs199473012	0.00004
NM_001010874.5(TECRL):c.587G>A (p.Arg196Gln)	rs773204795	0.00003
NM_000218.3(KCNQ1):c.1085A>G (p.Lys362Arg)	rs12720458	0.00001
NM_000335.5(SCN5A):c.1700T>A (p.Leu567Gln)	rs199473124	0.00001
NM_000218.3(KCNQ1):c.1024C>T (p.Leu342Phe)	rs199472760
NM_000218.3(KCNQ1):c.1049G>T (p.Gly350Val)	rs794728524
NM_000218.3(KCNQ1):c.1700T>C (p.Ile567Thr)	rs199472805
NM_000218.3(KCNQ1):c.373T>A (p.Tyr125Asn)	rs794728578
NM_000238.4(KCNH2):c.1595T>C (p.Leu532Pro)	rs1801182500
NM_000238.4(KCNH2):c.1874T>C (p.Val625Ala)	rs199472951
NM_000238.4(KCNH2):c.2453C>T (p.Ser818Leu)	rs121912510
NM_000238.4(KCNH2):c.66dup (p.Glu23Ter)	rs1554431441
NM_000891.3(KCNJ2):c.461G>A (p.Cys154Tyr)	rs199473380

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