ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.1971C>T (p.Tyr657=)

dbSNP: rs2042889723
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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 RCV001486679 SCV001691145 likely benign Brugada syndrome 8 2022-02-05 criteria provided, single submitter clinical testing

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