ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.5529-1076C>A

gnomAD frequency: 0.01911  dbSNP: rs17846920
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 RCV001654017 SCV001863668 benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001654017 SCV005315262 benign not provided criteria provided, single submitter not provided

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