Variants studied for Hearing loss, autosomal dominant 73

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
1	2	8	0	11	21

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
PTPRQ	1	2	8	11	21

Submitter and significance breakdown #

Total submitters: 11

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Genome-Nilou Lab	0	0	0	11	11
Institute of Human Genetics, University of Leipzig Medical Center	0	1	1	0	2
OMIM	1	0	0	0	1
Institute of Human Genetics, University of Goettingen	0	0	1	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	1	0	1
SIB Swiss Institute of Bioinformatics	0	0	1	0	1
Department of Biochemistry, Faculty of Medicine, University of Khartoum	0	0	1	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	1
Genomics England Pilot Project, Genomics England	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	0	1	0	1

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