ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.477+119988G>C

gnomAD frequency: 0.36354  dbSNP: rs4765905
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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 RCV001511447 SCV001718690 benign Long QT syndrome 2024-01-22 criteria provided, single submitter clinical testing

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