ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.659-18_659-17insC

gnomAD frequency: 0.00740  dbSNP: rs1554387291
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002073286 SCV002427174 benign Brugada syndrome 2025-01-28 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001699867 SCV001924576 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001699867 SCV001926791 benign not specified no assertion criteria provided clinical testing

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