ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.960A>G (p.Leu320=) (rs56093012)

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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	RCV000323678	SCV000338428	uncertain significance	not provided	2016-01-26	criteria provided, single submitter	clinical testing

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