ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.990G>C (p.Pro330=)

dbSNP: rs146954200
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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 RCV002073577 SCV002380408 likely benign Brugada syndrome 8 2021-07-27 criteria provided, single submitter clinical testing

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