ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.924C>T (p.Ile308=)

gnomAD frequency: 0.00002  dbSNP: rs1256500370
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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 RCV001455217 SCV001658975 likely benign Brugada syndrome 8 2025-01-23 criteria provided, single submitter clinical testing

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