ClinVar Miner

Variants studied for Autosomal recessive nonsyndromic hearing loss 2

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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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
59 38 245 33 49 411

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
MYO7A 59 38 245 33 49 411

Submitter and significance breakdown #

Total submitters: 27
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 208 29 14 251
Genome-Nilou Lab 2 1 24 4 42 73
Mendelics 8 2 5 0 5 20
Counsyl 5 12 1 0 0 18
King Laboratory, University of Washington 8 7 0 0 0 15
OMIM 6 0 0 0 0 6
Baylor Genetics 0 2 4 0 0 6
Laboratory of Prof. Karen Avraham, Tel Aviv University 6 0 0 0 0 6
Hereditary Research Laboratory, Bethlehem University 6 0 0 0 0 6
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital 4 2 0 0 0 6
WangQJ Lab, Chinese People's Liberation Army General Hospital 1 0 5 0 0 6
The Shared Resource Centre "Genome", Research Centre for Medical Genetics 2 4 0 0 0 6
National Institute on Deafness and Communication Disorders, National Institutes of Health 5 0 0 0 0 5
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital 2 1 2 0 0 5
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 2 2 0 0 0 4
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 3 0 0 3
Neuberg Centre For Genomic Medicine, NCGM 0 2 1 0 0 3
Genomics England Pilot Project, Genomics England 0 3 0 0 0 3
3billion 0 2 0 0 0 2
Dr.Nikuei Genetic Center 2 0 0 0 0 2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 1 0 0 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 1 0 0 0 0 1
Hereditary Risk Evalutation Team, Medical School Hannover 0 0 1 0 0 1
Breda Genetics srl 0 0 1 0 0 1
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 1 0 0 0 1
Palindrome, Gene Kavoshgaran Aria 1 0 0 0 0 1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) 1 0 0 0 0 1

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