ClinVar Miner

Submissions for variant NM_004369.3(COL6A3):c.5522T>G (p.Leu1841Arg) (rs886043336)

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	RCV000278642	SCV000339532	uncertain significance	not provided	2016-02-23	criteria provided, single submitter	clinical testing

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