ClinVar Miner

Submissions for variant NM_015295.2(SMCHD1):c.5597G>A (p.Arg1866Gln) (rs886044586)

Minimum review status:		Collection method:
Minimum conflict level:
		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	RCV000330129	SCV000345584	uncertain significance	not provided	2016-08-24	criteria provided, single submitter	clinical testing

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