List of variants reported as uncertain significance for long QT syndrome by MGZ Medical Genetics Center

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.526C>T (p.Arg176Trp)	rs36210422	0.00061
NM_000335.5(SCN5A):c.5333C>T (p.Thr1778Met)	rs199473634	0.00008
NM_001148.6(ANK2):c.7283C>T (p.Ser2428Leu)	rs772544901	0.00002
NM_000719.7(CACNA1C):c.5255C>T (p.Thr1752Ile)	rs752694570	0.00001
NM_000719.7(CACNA1C):c.1390+4A>G
NM_000719.7(CACNA1C):c.970C>T (p.Arg324Trp)	rs2154571835
NM_001354269.3(ANK2):c.23C>G (p.Ala8Gly)
NM_001743.6(CALM2):c.-56G>A
NM_005751.5(AKAP9):c.4175C>T (p.Thr1392Ile)
NM_005751.5(AKAP9):c.6148G>T (p.Asp2050Tyr)

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