ClinVar Miner

Submissions for variant NM_004369.3(COL6A3):c.5170G>A (p.Glu1724Lys) (rs398124122)

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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	RCV000080949	SCV000112856	uncertain significance	not provided	2012-11-05	criteria provided, single submitter	clinical testing

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