List of variants reported as pathogenic for long QT syndrome by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.673C>T (p.Arg225Trp)	rs199473072	0.00009
NM_000218.3(KCNQ1):c.1766G>A (p.Gly589Asp)	rs120074190	0.00006
NM_000238.4(KCNH2):c.1655T>C (p.Leu552Ser)	rs199472918	0.00006
NM_000218.3(KCNQ1):c.1552C>T (p.Arg518Ter)	rs17215500	0.00003
NM_000335.5(SCN5A):c.3953G>T (p.Gly1318Val)	rs199473220	0.00003
NM_000218.3(KCNQ1):c.1781G>A (p.Arg594Gln)	rs199472815	0.00001
NM_000218.3(KCNQ1):c.1066C>T (p.Gln356Ter)	rs397508072
NM_000218.3(KCNQ1):c.1124_1127del (p.Ile375fs)	rs397508077
NM_000218.3(KCNQ1):c.1343dup (p.Glu449fs)	rs397508087
NM_000218.3(KCNQ1):c.1893dup (p.Arg632fs)	rs397508104
NM_000218.3(KCNQ1):c.488del (p.Leu163fs)	rs397508112
NM_000218.3(KCNQ1):c.573_577del (p.Arg192fs)	rs397508118
NM_000219.6(KCNE1):c.292C>T (p.Arg98Trp)	rs199473362
NM_000238.4(KCNH2):c.1468G>A (p.Ala490Thr)	rs28928905
NM_000238.4(KCNH2):c.71_72insGC (p.Gln25fs)
NM_000335.5(SCN5A):c.664C>T (p.Arg222Ter)	rs794728849

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