ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.4624-47A>G

gnomAD frequency: 0.01074  dbSNP: rs114898435
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000861444 SCV001001754 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing

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