ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.864G>A (p.Lys288=)

gnomAD frequency: 0.00001  dbSNP: rs1296638967
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000793850 SCV000933226 likely benign Brugada syndrome 8 2024-12-12 criteria provided, single submitter clinical testing

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