List of variants reported as uncertain significance for long QT syndrome by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_172201.2(KCNE2):c.29C>T (p.Thr10Met)	rs199473648	0.00025
NM_000335.5(SCN5A):c.2066G>A (p.Arg689His)	rs199473145	0.00009
NM_000238.4(KCNH2):c.934C>T (p.Arg312Cys)	rs199472885	0.00008
NM_000219.6(KCNE1):c.29C>T (p.Thr10Met)	rs144917638	0.00007
NM_000335.5(SCN5A):c.5452G>A (p.Asp1818Asn)	rs137854619	0.00006
NM_000335.5(SCN5A):c.1915G>A (p.Gly639Arg)	rs199473136	0.00004
NM_000335.5(SCN5A):c.2102C>T (p.Pro701Leu)	rs199473147	0.00004
NM_000335.5(SCN5A):c.4475A>G (p.Lys1492Arg)	rs199473260	0.00004
NM_000219.6(KCNE1):c.292C>T (p.Arg98Trp)	rs199473362
NM_000335.5(SCN5A):c.2423G>A (p.Arg808His)	rs199473160
NM_000335.5(SCN5A):c.4591G>T (p.Val1531Phe)	rs199473618

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