ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.279+47T>G (rs115690090)

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	RCV000596251	SCV000700432	benign	not specified	2017-02-10	criteria provided, single submitter	clinical testing

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