List of variants reported as likely pathogenic for Long QT syndrome 2 by Blueprint Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000238.4(KCNH2):c.2738C>T (p.Ala913Val)	rs77331749	0.00056
NM_000238.4(KCNH2):c.1888G>A (p.Val630Ile)	rs199472958	0.00003
NM_000238.4(KCNH2):c.1352C>T (p.Pro451Leu)	rs199472902	0.00001
NM_000238.4(KCNH2):c.1402dup (p.Leu468fs)	rs869025448
NM_000238.4(KCNH2):c.1874T>C (p.Val625Ala)	rs199472951
NM_000238.4(KCNH2):c.774dup (p.Asp259fs)	rs869025447
NM_000238.4(KCNH2):c.842dup (p.Ala282fs)	rs730880374

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