ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.1407+297_1407+298insCCCC

gnomAD frequency: 0.14266 dbSNP: rs879827459

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	RCV001687969	SCV001910451	benign	not provided	2019-11-14	criteria provided, single submitter	clinical testing

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