ClinVar Miner

Submissions for variant NM_000392.5(ABCC2):c.213C>T (p.Phe71=) (rs770824435)

Minimum review status:		Collection method:
Minimum conflict level:
		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	RCV000731535	SCV000859367	uncertain significance	not provided	2018-01-25	criteria provided, single submitter	clinical testing

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