ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.4388+221_4388+233del

gnomAD frequency: 0.07853 dbSNP: rs745747852

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
GeneDx	RCV001643257	SCV001857780	benign	not provided	2019-08-18	criteria provided, single submitter	clinical testing

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