ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1054+7C>T

gnomAD frequency: 0.19120  dbSNP: rs4314963
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245077 SCV000317160 benign not specified criteria provided, single submitter clinical testing
Invitae RCV000860377 SCV001000414 benign Brugada syndrome 4 2024-02-01 criteria provided, single submitter clinical testing
GeneDx RCV001711843 SCV001945255 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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