ClinVar Miner

Submissions for variant NM_000722.4(CACNA2D1):c.3160-9del

dbSNP: rs367960608
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001513155 SCV001720704 benign Brugada syndrome 2023-11-15 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001700766 SCV001923667 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001702600 SCV001928847 likely benign not provided no assertion criteria provided clinical testing

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