List of variants reported as not provided for long QT syndrome by GenomeConnect, ClinGen

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.2863C>G (p.Leu955Val)	rs199473012	0.00004
NM_000238.4(KCNH2):c.3457C>T (p.His1153Tyr)	rs199473035	0.00002
NM_001148.6(ANK2):c.10080G>C (p.Gln3360His)	rs1214575789	0.00001
NM_001148.6(ANK2):c.109C>T (p.Arg37Cys)	rs369877280	0.00001
NM_000238.4(KCNH2):c.1926C>G (p.Ile642Met)	rs1801154313
NM_000238.4(KCNH2):c.2464G>A (p.Val822Met)	rs121912506
NM_000238.4(KCNH2):c.3002G>A (p.Trp1001Ter)	rs794728401
NM_000335.5(SCN5A):c.1076C>A (p.Ala359Asp)	rs1553704925
NM_000891.3(KCNJ2):c.431G>A (p.Gly144Asp)	rs199473377
NM_001148.6(ANK2):c.1069C>T (p.Pro357Ser)	rs2049005904
NM_001148.6(ANK2):c.4351A>G (p.Thr1451Ala)	rs1554536556
NM_001148.6(ANK2):c.7942G>C (p.Gly2648Arg)	rs199828363

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