ClinVar Miner

Submissions for variant NM_000238.4(KCNH2):c.2146-18C>T

gnomAD frequency: 0.00001  dbSNP: rs770433324
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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 RCV002134142 SCV002459747 likely benign Long QT syndrome 2023-04-01 criteria provided, single submitter clinical testing

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