ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.837A>T (p.Glu279Asp) (rs773509355)

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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	RCV000595634	SCV000707380	uncertain significance	not provided	2017-03-27	criteria provided, single submitter	clinical testing

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