ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.4314C>T (p.Ser1438=) (rs376790802)

Minimum review status:		Collection method:
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		ClinVar version:

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	RCV000177511	SCV000229393	uncertain significance	not provided	2017-12-07	criteria provided, single submitter	clinical testing

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