Variants studied for Autosomal recessive nonsyndromic hearing loss 86

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	not provided	total
6	1	5	0	0	1	13

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	not provided	total
TBC1D24	6	1	4	1	12
CCNF, TBC1D24	0	0	1	0	1

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	not provided	total
OMIM	2	0	0	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	1	0	0	2
Department of Molecular and Human Genetics, Baylor College of Medicine	2	0	0	0	2
Center of Genomic medicine, Geneva, University Hospital of Geneva	0	0	2	0	2
Division of Medical Genetics; Sainte-Justine Hospital	2	0	0	0	2
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital	0	0	2	0	2
Genomic Research Center, Shahid Beheshti University of Medical Sciences	1	0	0	0	1
Molecular Biology of Hearing and Deafness Laboratory, Xinhua Hospital	0	0	0	1	1
National Institute on Deafness and Communication Disorders, National Institutes of Health	1	0	0	0	1
Laboratory of Prof. Karen Avraham, Tel Aviv University	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	1

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