ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.*10G>T

gnomAD frequency: 0.76187  dbSNP: rs4747352
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000195586 SCV000252900 benign Brugada syndrome 4 2015-06-26 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000249061 SCV000317155 benign not specified criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000195586 SCV000743848 benign Brugada syndrome 4 2014-10-09 criteria provided, single submitter clinical testing
GeneDx RCV001636718 SCV001847952 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000195586 SCV000732937 benign Brugada syndrome 4 no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV000249061 SCV001925985 benign not specified no assertion criteria provided clinical testing

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