List of variants reported as uncertain significance for Long QT syndrome 3 by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.659C>T (p.Thr220Ile)	rs45620037	0.00068
NM_000335.5(SCN5A):c.1844G>A (p.Gly615Glu)	rs12720452	0.00030
NM_000335.5(SCN5A):c.1943C>T (p.Pro648Leu)	rs45609733	0.00019
NM_000335.5(SCN5A):c.5333C>T (p.Thr1778Met)	rs199473634	0.00008
NM_000335.5(SCN5A):c.880G>A (p.Val294Met)	rs199473086	0.00004
NM_000335.5(SCN5A):c.2924G>A (p.Arg975Gln)	rs753149586	0.00003
NM_000335.5(SCN5A):c.6031C>T (p.Arg2011Cys)	rs199473640	0.00002
NM_000335.5(SCN5A):c.1298G>A (p.Arg433His)	rs879035421	0.00001
NM_000335.5(SCN5A):c.2078G>T (p.Arg693Leu)	rs373087176
NM_000335.5(SCN5A):c.2437-7T>C	rs1012068196
NM_000335.5(SCN5A):c.2643G>T (p.Met881Ile)	rs1559756973
NM_000335.5(SCN5A):c.3304T>G (p.Ser1102Ala)	rs1575757097
NM_000335.5(SCN5A):c.4390T>C (p.Phe1464Leu)	rs1559728884
NM_000335.5(SCN5A):c.4502G>A (p.Gly1501Asp)	rs1230010586
NM_000335.5(SCN5A):c.4598T>G (p.Ile1533Ser)	rs1575712112
NM_000335.5(SCN5A):c.4787T>C (p.Val1596Ala)

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