ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.2211C>G (p.Val737=)

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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 RCV005142611 SCV005756551 likely benign Brugada syndrome 2024-07-11 criteria provided, single submitter clinical testing

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