ClinVar Miner

Submissions for variant NM_000726.5(CACNB4):c.*151dup

dbSNP: rs79470866
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000403497 SCV000417226 uncertain significance Hereditary episodic ataxia 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000308121 SCV000417227 uncertain significance Juvenile myoclonic epilepsy 2016-06-14 criteria provided, single submitter clinical testing

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