ClinVar Miner

Submissions for variant NM_172057.2(KCNH2):c.2059C>A (p.Leu687Ile) (rs794728346)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000181740 SCV000234043 likely benign Cardiac arrhythmia 2014-09-18 criteria provided, single submitter clinical testing The variant is found in LQT panel(s).

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