ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.9475C>T (p.Leu3159=)

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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 RCV003092677 SCV003477143 likely benign Long QT syndrome 2022-02-21 criteria provided, single submitter clinical testing

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