ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.1738-13C>T

dbSNP: rs2151215519
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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 RCV002212592 SCV002362379 likely benign Brugada syndrome 8 2024-08-03 criteria provided, single submitter clinical testing

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