ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.3424G>C (p.Val1142Leu) (rs375280444)

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	RCV000595615	SCV000704007	uncertain significance	not provided	2016-11-22	criteria provided, single submitter	clinical testing

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