Variants studied for Autosomal recessive nonsyndromic hearing loss 25

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
10	3	18	1	5	35

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
GRXCR1	10	3	18	1	5	35

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	17	1	5	23
OMIM	4	0	0	0	0	4
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	2	0	0	2
Institute of Rare Diseases, West China Hospital, Sichuan University	2	0	0	0	0	2
Baylor Genetics	1	0	0	0	0	1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	1	0	0	0	0	1
Fulgent Genetics, Fulgent Genetics	0	1	0	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	1	0	0	0	0	1
King Laboratory, University of Washington	0	1	0	0	0	1
National Institute on Deafness and Communication Disorders, National Institutes of Health	1	0	0	0	0	1
Payam Genetics Center, General Welfare Department of North Khorasan Province	1	0	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	0	1	0	0	0	1

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