List of variants reported as likely pathogenic for long QT syndrome by SIB Swiss Institute of Bioinformatics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.5347G>A (p.Glu1783Lys)	rs137854601	0.00001
NM_000218.3(KCNQ1):c.1016T>C (p.Phe339Ser)	rs199472759
NM_000238.4(KCNH2):c.2510A>G (p.Asp837Gly)	rs199473004
NM_006888.6(CALM1):c.268T>C (p.Phe90Leu)	rs730882253

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