ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.3531G>A (p.Gly1177=)

dbSNP: rs375911378
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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 RCV000870299 SCV001011790 likely benign Brugada syndrome 8 2023-05-05 criteria provided, single submitter clinical testing

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