ClinVar Miner

Submissions for variant NM_001040151.2(SCN3B):c.445+20T>G

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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 RCV003860115 SCV004661916 likely benign Brugada syndrome 7 2024-01-03 criteria provided, single submitter clinical testing

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