ClinVar Miner

Submissions for variant NM_201590.3(CACNB2):c.*10G>T (rs4747352)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen RCV000195586 SCV000732937 benign Brugada syndrome 4 no assertion criteria provided clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000195586 SCV000743848 benign Brugada syndrome 4 2014-10-09 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000281086 SCV000361823 likely benign Brugada syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000195586 SCV000252900 benign Brugada syndrome 4 2015-06-26 criteria provided, single submitter clinical testing
PreventionGenetics RCV000249061 SCV000317155 benign not specified criteria provided, single submitter clinical testing

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