List of variants reported as likely pathogenic for long QT syndrome by MVZ Medizinische Genetik Mainz

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.124A>T (p.Ile42Phe)
NM_000238.4(KCNH2):c.1592G>C (p.Arg531Pro)
NM_000719.7(CACNA1C):c.788A>T (p.Lys263Met)

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