ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.1113+23C>A

gnomAD frequency: 0.00166  dbSNP: rs142826660
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000860639 SCV001000751 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707415 SCV005234222 benign not provided criteria provided, single submitter not provided

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