ClinVar Miner

Submissions for variant NM_001205293.3(CACNA1E):c.1315+168A>T

gnomAD frequency: 0.05806  dbSNP: rs866126891
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 RCV001688865 SCV001915530 benign not provided 2021-04-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001688865 SCV005282393 benign not provided criteria provided, single submitter not provided

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