Variants studied for Autosomal dominant nonsyndromic hearing loss 13

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
2	6	14	0	15	37

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
COL11A2	2	6	14	15	37

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Genome-Nilou Lab	0	0	0	15	15
Institute of Human Genetics, University of Leipzig Medical Center	0	0	3	0	3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	3	0	3
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	1	1	0	2
OMIM	2	0	0	0	2
3billion	0	0	1	0	1
Baylor Genetics	0	0	1	0	1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS)	0	1	0	0	1
Division of Human Genetics, Children's Hospital of Philadelphia	0	0	1	0	1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	0	0	1	0	1
Institute of Human Genetics, University of Goettingen	0	1	0	0	1
Institute of Rare Diseases, West China Hospital, Sichuan University	0	1	0	0	1
King Laboratory, University of Washington	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	0	1	0	1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota	0	1	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	1
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas	0	0	1	0	1

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