ClinVar Miner

Submissions for variant NM_015295.2(SMCHD1):c.3625A>G (p.Thr1209Ala)

Minimum review status:		Collection method:
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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	RCV000728015	SCV000855533	uncertain significance	not provided	2017-07-10	criteria provided, single submitter	clinical testing

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