ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.1926A>G (p.Glu642=)

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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 RCV003017679 SCV003325527 likely benign Brugada syndrome 2022-05-05 criteria provided, single submitter clinical testing

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