List of variants reported as likely pathogenic for Long QT syndrome 3

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.3908C>T (p.Thr1303Met)	rs199473603	0.00021
NM_000335.5(SCN5A):c.3157G>A (p.Glu1053Lys)	rs137854617	0.00016
NM_000335.5(SCN5A):c.4475A>G (p.Lys1492Arg)	rs199473260	0.00004
NM_000335.5(SCN5A):c.4874G>A (p.Arg1625His)	rs199473283	0.00004
NM_000335.5(SCN5A):c.4498C>G (p.Leu1500Val)	rs199473266	0.00002
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.5347G>A (p.Glu1783Lys)	rs137854601	0.00001
NM_000335.5(SCN5A):c.674G>A (p.Arg225Gln)	rs199473071	0.00001
NM_000335.5(SCN5A):c.3944G>T (p.Arg1315Leu)	rs765907469
NM_000335.5(SCN5A):c.4460C>A (p.Thr1487Lys)	rs199473259
NM_000335.5(SCN5A):c.4844TCT[1] (p.Phe1616del)	rs749697698
NM_000335.5(SCN5A):c.4865G>T (p.Arg1622Leu)	rs137854600
NM_000335.5(SCN5A):c.5354T>C (p.Leu1785Pro)	rs199473315

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