Submissions for variant NM_014927.5(CNKSR2):c.2199G>A (p.Thr733=)

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

Total submissions: 2

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Eurofins Ntd Llc (ga)	RCV000081682	SCV000113613	uncertain significance	not provided	2013-10-31	criteria provided, single submitter	clinical testing
Labcorp Genetics (formerly Invitae), Labcorp	RCV000081682	SCV001045598	benign	not provided	2019-12-31	criteria provided, single submitter	clinical testing

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