ClinVar Miner

Submissions for variant NM_004369.3(COL6A3):c.4848C>T (p.Ser1616=) (rs200948078)

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	RCV000080944	SCV000112851	uncertain significance	not provided	2018-07-02	criteria provided, single submitter	clinical testing

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