ClinVar Miner

Submissions for variant NM_001148.6(ANK2):c.8891T>C (p.Ile2964Thr)

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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 RCV003648637 SCV004469222 benign Long QT syndrome 2023-11-27 criteria provided, single submitter clinical testing

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