ClinVar Miner

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

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Total variants: 7
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HGVS dbSNP
NM_000335.4(SCN5A):c.3908C>T (p.Thr1303Met) rs199473603
NM_198056.2(SCN5A):c.3157G>A (p.Glu1053Lys) rs137854617
NM_198056.2(SCN5A):c.4463C>A (p.Thr1488Lys)
NM_198056.2(SCN5A):c.4501C>G (p.Leu1501Val) rs199473266
NM_198056.2(SCN5A):c.4850_4852delTCT (p.Phe1617del) rs749697698
NM_198056.2(SCN5A):c.4886G>A (p.Arg1629Gln) rs199473623
NM_198056.2(SCN5A):c.5350G>A (p.Glu1784Lys) rs137854601

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