ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.186G>A (p.Ala62=)

gnomAD frequency: 0.00001  dbSNP: rs1196730430
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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 RCV001233841 SCV001406455 likely benign Brugada syndrome 8 2024-08-29 criteria provided, single submitter clinical testing

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