Variants studied for autosomal recessive nonsyndromic hearing loss 42

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
11	3	9	0	3	25

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
ILDR1	11	3	9	3	25

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Fulgent Genetics, Fulgent Genetics	0	1	3	1	5
OMIM	4	0	0	0	4
Revvity Omics, Revvity	2	1	1	0	4
3billion	2	1	0	0	3
King Laboratory, University of Washington	2	0	0	0	2
National Institute on Deafness and Communication Disorders, National Institutes of Health	2	0	0	0	2
Genome-Nilou Lab	0	0	0	2	2
Baylor Genetics	0	0	1	0	1
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	1	0	1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	1	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	1
Knight Diagnostic Laboratories, Oregon Health and Sciences University	0	0	1	0	1
Center of Genomic medicine, Geneva, University Hospital of Geneva	1	0	0	0	1
Juno Genomics, Hangzhou Juno Genomics, Inc	0	1	0	0	1
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital	1	0	0	0	1
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	0	0	1	0	1
Department of Human Genetics, Hannover Medical School	0	0	1	0	1

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