ClinVar Miner

Submissions for variant NM_015295.2(SMCHD1):c.4738A>G (p.Ser1580Gly) (rs886044485)

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	RCV000262528	SCV000345122	uncertain significance	not provided	2016-09-01	criteria provided, single submitter	clinical testing

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