ClinVar Miner

Submissions for variant NM_000726.4(CACNB4):c.-70G>A

dbSNP: rs183873853
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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 RCV000393297 SCV000483881 likely benign Juvenile myoclonic epilepsy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000314711 SCV000483882 likely benign Hereditary episodic ataxia 2016-06-14 criteria provided, single submitter clinical testing

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