ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.1668G>A (p.Glu556=)

dbSNP: rs2151215619
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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 RCV001438434 SCV001641306 likely benign Brugada syndrome 8 2022-07-25 criteria provided, single submitter clinical testing

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