ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.1978+11C>T

gnomAD frequency: 0.00001  dbSNP: rs1370545147
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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 RCV002071616 SCV002428579 likely benign Brugada syndrome 8 2022-05-27 criteria provided, single submitter clinical testing

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