Variants studied for Autosomal recessive nonsyndromic hearing loss 59

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
15	1	39	2	2	57

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
PJVK	15	1	39	1	2	56
PJVK, PRKRA	0	0	0	1	0	1

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	34	2	0	36
OMIM	7	0	0	0	0	7
Genetics Department, Hospital Ramon y Cajal-IRYCIS	4	0	0	0	0	4
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	3	0	0	0	0	3
Fulgent Genetics, Fulgent Genetics	0	0	2	0	0	2
Genome-Nilou Lab	0	0	0	0	2	2
King Laboratory, University of Washington	1	0	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	0	1	0	0	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	0	1	0	0	1
National Institute on Deafness and Communication Disorders, National Institutes of Health	1	0	0	0	0	1
Breda Genetics srl	0	0	1	0	0	1
3billion	1	0	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	0	1
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital	0	0	1	0	0	1

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