ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.2991C>T (p.Pro997=)

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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 RCV005150820 SCV005774157 likely benign Brugada syndrome 8 2025-01-11 criteria provided, single submitter clinical testing

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