List of variants reported as uncertain significance for long QT syndrome by Dr. med. U. Finckh, Human Genetics, Eurofins MVZ

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001148.6(ANK2):c.6100G>A (p.Gly2034Arg)	rs764677814	0.00002
NM_000719.7(CACNA1C):c.2181G>T (p.Met727Ile)
NM_000719.7(CACNA1C):c.4784G>A (p.Arg1595Gln)	rs1313283709
NM_001148.6(ANK2):c.3741G>A (p.Met1247Ile)

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