ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.579A>G (p.Leu193=)

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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 RCV003539675 SCV004269494 likely benign Brugada syndrome 2023-12-29 criteria provided, single submitter clinical testing

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