List of variants reported as pathogenic for long QT syndrome by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1876G>A (p.Gly626Ser)	rs199472821	0.00001
NM_000335.5(SCN5A):c.1604G>A (p.Arg535Gln)	rs199473121	0.00001
NM_000891.3(KCNJ2):c.269T>G (p.Leu90Arg)

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