ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.293+182T>C

gnomAD frequency: 0.00671  dbSNP: rs144454175
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001571435 SCV001795915 likely benign not provided 2018-07-26 criteria provided, single submitter clinical testing

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