ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.1059A>G (p.Glu353=)

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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 RCV005118741 SCV005742637 likely benign Brugada syndrome 2024-02-22 criteria provided, single submitter clinical testing

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