ClinVar Miner

Submissions for variant NM_004369.3(COL6A3):c.8256G>A (p.Leu2752=) (rs769124771)

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	RCV000330418	SCV000336427	uncertain significance	not provided	2015-10-07	criteria provided, single submitter	clinical testing

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