List of variants reported as likely pathogenic for long QT syndrome by Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine

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Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000219.6(KCNE1):c.226G>A (p.Asp76Asn)	rs74315445	0.00005
NM_000238.4(KCNH2):c.1888G>A (p.Val630Ile)	rs199472958	0.00003
NM_000335.5(SCN5A):c.4498C>G (p.Leu1500Val)	rs199473266	0.00002
NM_000218.3(KCNQ1):c.1664G>A (p.Arg555His)	rs199472800	0.00001
NM_000218.3(KCNQ1):c.776G>A (p.Arg259His)	rs199472720	0.00001
NM_000218.3(KCNQ1):c.905C>T (p.Ala302Val)	rs193922365	0.00001
NM_000335.5(SCN5A):c.2441G>A (p.Arg814Gln)	rs199473584	0.00001
NM_000335.5(SCN5A):c.4883G>A (p.Arg1628Gln)	rs199473623	0.00001
NM_000335.5(SCN5A):c.4892G>A (p.Arg1631His)	rs199473286	0.00001
NM_000218.3(KCNQ1):c.425del (p.Leu142fs)	rs794728566
NM_000218.3(KCNQ1):c.532G>A (p.Ala178Thr)	rs120074177
NM_000218.3(KCNQ1):c.843C>A (p.Tyr281Ter)	rs1057520623
NM_000218.3(KCNQ1):c.944A>G (p.Tyr315Cys)	rs74462309
NM_000238.4(KCNH2):c.1468G>A (p.Ala490Thr)	rs28928905
NM_000238.4(KCNH2):c.215C>A (p.Pro72Gln)	rs199473421
NM_000238.4(KCNH2):c.245T>C (p.Ile82Thr)	rs1563189895
NM_000335.5(SCN5A):c.2335del (p.Gln779fs)	rs2061687300
NM_000335.5(SCN5A):c.4780G>C (p.Asp1594His)	rs137854607

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