ClinVar Miner

Submissions for variant NM_005477.3(HCN4):c.3174C>T (p.Ser1058=)

dbSNP: rs2151214056
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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 RCV002198831 SCV002492252 likely benign Brugada syndrome 8 2023-03-26 criteria provided, single submitter clinical testing

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