ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.2523G>T (p.Ser841=)

dbSNP: rs768157473
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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 RCV001408426 SCV001610426 likely benign Brugada syndrome 8 2019-09-07 criteria provided, single submitter clinical testing

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