ClinVar Miner

Submissions for variant NM_033100.4(CDHR1):c.2246_2253del (p.Arg749fs) (rs886044648)

Minimum review status:		Collection method:
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		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics	RCV000359142	SCV000345785	likely pathogenic	not provided	2016-09-02	criteria provided, single submitter	clinical testing

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