List of variants reported as uncertain significance for long QT syndrome by Institute of Human Genetics, University of Goettingen

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000218.3(KCNQ1):c.1882G>A (p.Gly628Ser)	rs745990205	0.00002
NM_003098.3(SNTA1):c.25C>T (p.Arg9Cys)	rs886039012	0.00002
NM_001148.6(ANK2):c.767G>C (p.Gly256Ala)	rs1276798019	0.00001
NM_000335.5(SCN5A):c.3866C>T (p.Thr1289Ile)	rs2125844123
NM_000719.7(CACNA1C):c.4436T>C (p.Phe1479Ser)	rs2096050688
NM_172201.2(KCNE2):c.247C>G (p.Pro83Ala)	rs1979548748

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