List of variants reported as likely pathogenic for long QT syndrome by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.1888G>A (p.Val630Ile)	rs199472958	0.00003
NM_000218.3(KCNQ1):c.898G>A (p.Ala300Thr)	rs120074187	0.00002
NM_000335.5(SCN5A):c.4498C>G (p.Leu1500Val)	rs199473266	0.00002
NM_000218.3(KCNQ1):c.1085A>G (p.Lys362Arg)	rs12720458	0.00001
NM_000218.3(KCNQ1):c.1515-2_1515-1del	rs1564886323
NM_000218.3(KCNQ1):c.1686-2A>G	rs878854350
NM_000218.3(KCNQ1):c.1697C>T (p.Ser566Phe)	rs199472804
NM_000218.3(KCNQ1):c.387-5T>A	rs794728549
NM_000218.3(KCNQ1):c.724G>T (p.Asp242Tyr)	rs199472712
NM_000238.4(KCNH2):c.2162C>T (p.Pro721Leu)	rs199472986
NM_000238.4(KCNH2):c.2398+5G>T	rs1554425149
NM_000238.4(KCNH2):c.98A>C (p.Asn33Thr)	rs199473487
NM_000335.5(SCN5A):c.1338+2T>A	rs786204839
NM_000335.5(SCN5A):c.3509-1G>C	rs1553698563
NM_001005242.3(PKP2):c.2311_2316delinsGAAA (p.Asn771fs)	rs786204395
NM_033337.3(CAV3):c.213G>A (p.Trp71Ter)	rs2124988406

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