Variants studied for Usher syndrome type 3

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
17	15	58	10	7	103

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
CLRN1	17	15	58	10	7	103

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	1	0	36	4	7	48
Counsyl	2	13	11	5	1	32
Natera, Inc.	4	0	11	1	0	16
OMIM	8	0	0	0	0	8
Sharon lab, Hadassah-Hebrew University Medical Center	4	1	0	0	0	5
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	4	0	0	0	0	4
Centre for Genomic Medicine, Manchester, Central Manchester University Hospitals	3	0	0	0	0	3
Baylor Genetics	1	1	0	0	0	2
National Institute on Deafness and Communication Disorders, National Institutes of Health	2	0	0	0	0	2
The Cell Therapy Center, The University of Jordan	2	0	0	0	0	2
Genetic Services Laboratory, University of Chicago	1	0	0	0	0	1
Mendelics	0	1	0	0	0	1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	0	1	0	0	1
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+	1	0	0	0	0	1
Reproductive Health Research and Development, BGI Genomics	1	0	0	0	0	1
Myriad Genetics, Inc.	1	0	0	0	0	1

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