ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.117C>T (p.Gly39=)

gnomAD frequency: 0.00003  dbSNP: rs1009333860
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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 RCV002147405 SCV002416638 likely benign Brugada syndrome 8 2022-04-04 criteria provided, single submitter clinical testing

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