ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.121-9_121-3del

dbSNP: rs71402148
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000625135 SCV000743840 likely benign Brugada syndrome 4 2017-07-12 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV001701412 SCV001923695 benign not specified no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001700267 SCV001926636 likely benign not provided no assertion criteria provided clinical testing

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