ClinVar Miner

Submissions for variant NM_006514.4(SCN10A):c.692-7C>T

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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 RCV005174467 SCV005804620 likely benign Brugada syndrome 2024-09-09 criteria provided, single submitter clinical testing

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