ClinVar Miner

Submissions for variant NM_147127.5(EVC2):c.3557+138dup

gnomAD frequency: 0.01005 dbSNP: rs201389445

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	RCV001586512	SCV001813028	likely benign	not provided	2019-03-16	criteria provided, single submitter	clinical testing

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