Variants studied for autosomal recessive nonsyndromic hearing loss 35

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
6	2	61	4	7	78

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
ESRRB	6	2	61	4	7	78

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	59	3	6	68
OMIM	3	0	0	0	0	3
Baylor Genetics	0	1	2	0	0	3
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	1	1	1	3
Hereditary Research Laboratory, Bethlehem University	2	0	0	0	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	1	0	0	0	1
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine	0	0	1	0	0	1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center	0	0	1	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
Department of Medical Genetics, Tabriz University of Medical Sciences	1	0	0	0	0	1

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