List of variants reported as pathogenic for long QT syndrome by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.502G>A (p.Gly168Arg)	rs179489	0.00001
NM_000218.3(KCNQ1):c.604G>A (p.Asp202Asn)	rs199472702	0.00001
NM_000238.4(KCNH2):c.2230C>T (p.Arg744Ter)	rs189014161
NM_000238.4(KCNH2):c.2616del (p.Gly873fs)
NM_000238.4(KCNH2):c.418del (p.Ser140fs)	rs2117011793

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