ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.3558+10dup

gnomAD frequency: 0.00001  dbSNP: rs1555884916
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001424650 SCV001627249 likely benign Long QT syndrome 2020-01-29 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003736787 SCV004563748 likely benign not provided 2023-11-22 criteria provided, single submitter clinical testing

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