ClinVar Miner

Submissions for variant NM_000719.7(CACNA1C):c.5445-262A>G

gnomAD frequency: 0.05988  dbSNP: rs35176240
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000860305 SCV001000318 benign Long QT syndrome 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV001675967 SCV001895172 benign not provided 2018-06-23 criteria provided, single submitter clinical testing

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