ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1054+18G>A

gnomAD frequency: 0.00039  dbSNP: rs192538011
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001797961 SCV002041846 benign not specified 2021-11-29 criteria provided, single submitter clinical testing
Invitae RCV002074133 SCV002454023 benign Brugada syndrome 4 2023-12-05 criteria provided, single submitter clinical testing

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