ClinVar Miner

Variants studied for Autosomal recessive nonsyndromic hearing loss 30

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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
14 15 119 14 31 182

Gene and significance breakdown #

Total genes and gene combinations: 1
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
MYO3A 14 15 119 14 31 182

Submitter and significance breakdown #

Total submitters: 27
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 101 11 17 129
Genome-Nilou Lab 0 0 0 0 20 20
Department of Pathology and Laboratory Medicine, Sinai Health System 0 2 11 0 0 13
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 1 3 0 7 11
Fulgent Genetics, Fulgent Genetics 0 0 8 2 0 10
Revvity Omics, Revvity 1 2 3 1 0 7
OMIM 3 0 0 0 0 3
Mendelics 1 0 0 0 2 3
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital 2 1 0 0 0 3
Neuberg Centre For Genomic Medicine, NCGM 0 3 0 0 0 3
Institute of Rare Diseases, West China Hospital, Sichuan University 1 2 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 1 0 0 0 2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 1 1 0 2
Juno Genomics, Hangzhou Juno Genomics, Inc 0 2 0 0 0 2
3billion 2 0 0 0 0 2
Baylor Genetics 0 0 1 0 0 1
King Laboratory, University of Washington 1 0 0 0 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 0 0 1 0 0 1
Laboratory of Prof. Karen Avraham, Tel Aviv University 1 0 0 0 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 0 1
Centre for Arab Genomic Studies, Sheikh Hamdan Award for Medical Sciences 1 0 0 0 0 1
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill 0 1 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 0 1 0 0 1
WangQJ Lab, Chinese People's Liberation Army General Hospital 0 1 0 0 0 1
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital 1 0 0 0 0 1
Dr.Nikuei Genetic Center 0 1 0 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.