ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.2021-14del

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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 RCV002912787 SCV003246870 benign Brugada syndrome 2022-10-17 criteria provided, single submitter clinical testing

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