Submissions for variant NM_001127898.4(CLCN5):c.1609C>T (p.Arg537Ter) (rs797044811)

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 2

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
GeneReviews	RCV000192277	SCV000243785	pathogenic	Dent disease type 1	2014-09-25	no assertion criteria provided	literature only
Gharavi Laboratory,Columbia University	RCV000681792	SCV000809257	pathogenic	not provided	2018-09-16	no assertion criteria provided	research

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