ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.2686G>A (p.Glu896Lys) (rs377107178)

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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	RCV000593294	SCV000706220	uncertain significance	not provided	2018-04-12	criteria provided, single submitter	clinical testing

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