ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.804+653G>A

gnomAD frequency: 0.00292  dbSNP: rs142899184
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section, National Institutes of Health RCV000171803 SCV000050762 benign not specified 2013-06-24 criteria provided, single submitter research
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001849 SCV001159551 likely benign Brugada syndrome 4 2023-11-29 criteria provided, single submitter clinical testing
GeneDx RCV001711345 SCV001945251 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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