List of variants reported as likely pathogenic for long QT syndrome by Laan Lab, Human Genetics Research Group, University of Tartu

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.4874G>A (p.Arg1625His)	rs199473283	0.00004
NM_000218.3(KCNQ1):c.568C>T (p.Arg190Trp)	rs199473662

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