ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.1489-248T>C

gnomAD frequency: 0.03752  dbSNP: rs116757902
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001641042 SCV001856781 benign not provided 2019-08-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001641042 SCV005320480 benign not provided criteria provided, single submitter not provided

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