ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.1806G>A (p.Leu602=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003531739 SCV004314586 likely benign Long QT syndrome 2023-07-31 criteria provided, single submitter clinical testing

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