List of variants reported as likely pathogenic for long QT syndrome by All of Us Research Program, National Institutes of Health

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Total variants: 25

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1085A>G (p.Lys362Arg)	rs12720458	0.00001
NM_000218.3(KCNQ1):c.604G>A (p.Asp202Asn)	rs199472702	0.00001
NM_000218.3(KCNQ1):c.683+5G>A	rs397508122	0.00001
NM_000218.3(KCNQ1):c.905C>T (p.Ala302Val)	rs193922365	0.00001
NM_000238.4(KCNH2):c.1979C>T (p.Ser660Leu)	rs199472979	0.00001
NM_000335.5(SCN5A):c.1099C>T (p.Arg367Cys)	rs199473097	0.00001
NM_000218.3(KCNQ1):c.1252-1G>A
NM_000218.3(KCNQ1):c.1393+1G>A
NM_000218.3(KCNQ1):c.1480G>T (p.Glu494Ter)
NM_000218.3(KCNQ1):c.1663C>A (p.Arg555Ser)	rs120074185
NM_000218.3(KCNQ1):c.1892_1911del (p.Pro631fs)	rs397508103
NM_000218.3(KCNQ1):c.1893del (p.Arg632fs)	rs397508104
NM_000218.3(KCNQ1):c.387-5T>A	rs794728549
NM_000218.3(KCNQ1):c.556G>A (p.Gly186Ser)	rs199473398
NM_000218.3(KCNQ1):c.564G>A (p.Trp188Ter)	rs530612385
NM_000218.3(KCNQ1):c.566G>A (p.Gly189Glu)	rs199473400
NM_000218.3(KCNQ1):c.905C>A (p.Ala302Glu)	rs193922365
NM_000218.3(KCNQ1):c.921+1G>T	rs397508130
NM_000218.3(KCNQ1):c.928G>A (p.Val310Ile)	rs199472745
NM_000238.4(KCNH2):c.1128G>A (p.Gln376=)	rs770047651
NM_000238.4(KCNH2):c.1591C>T (p.Arg531Trp)	rs199472915
NM_000238.4(KCNH2):c.2453C>G (p.Ser818Trp)
NM_000238.4(KCNH2):c.2510A>G (p.Asp837Gly)	rs199473004
NM_000335.5(SCN5A):c.2204C>T (p.Ala735Val)	rs137854611
NM_000335.5(SCN5A):c.3273del (p.Arg1092fs)

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