ClinVar Miner

Submissions for variant NM_201596.3(CACNB2):c.*52_*55dup

gnomAD frequency: 0.00761  dbSNP: rs199830080
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001768137 SCV002008569 likely benign not provided 2018-12-31 criteria provided, single submitter clinical testing

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