ClinVar Miner

Submissions for variant NM_000092.5(COL4A4):c.2861-311_2861-310insG

gnomAD frequency: 0.79576 dbSNP: rs3835891

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	RCV001654325	SCV001864497	benign	not provided	2018-07-09	criteria provided, single submitter	clinical testing

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