ClinVar Miner

Submissions for variant NM_000218.3(KCNQ1):c.1251+7A>G

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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 RCV002663659 SCV002983711 likely benign Long QT syndrome 2022-04-17 criteria provided, single submitter clinical testing

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