ClinVar Miner

Submissions for variant NM_005184.4(CALM3):c.178+19G>A

gnomAD frequency: 0.00001  dbSNP: rs186405375
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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 RCV002204571 SCV002357317 benign Long QT syndrome 1 2023-12-19 criteria provided, single submitter clinical testing

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