ClinVar Miner

Submissions for variant NM_001377540.1(SLMAP):c.1794A>C (p.Arg598=)

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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 RCV003822372 SCV004619046 likely benign Brugada syndrome 2023-11-02 criteria provided, single submitter clinical testing

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