ClinVar Miner

Variants studied for autosomal dominant nonsyndromic hearing loss 22

Included ClinVar conditions (2):
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
12 8 111 25 52 208

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
MYO6 12 8 111 25 52 208

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 94 25 49 168
Fulgent Genetics, Fulgent Genetics 1 0 4 0 4 9
Juno Genomics, Hangzhou Juno Genomics, Inc 0 1 4 0 0 5
Laboratory of Prof. Karen Avraham, Tel Aviv University 4 0 0 0 0 4
OMIM 3 0 0 0 0 3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 2 0 1 0 0 3
Genome-Nilou Lab 0 0 0 0 3 3
MGZ Medical Genetics Center 0 1 1 0 0 2
King Laboratory, University of Washington 0 1 0 0 0 1
Mendelics 0 0 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 0 1 0 0 1
Division of Human Genetics, Children's Hospital of Philadelphia 0 0 1 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 0 0 1 0 0 1
Hereditary Research Laboratory, Bethlehem University 1 0 0 0 0 1
Institute of Human Genetics, University of Wuerzburg 0 0 1 0 0 1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 1 0 0 0 0 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 1 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 0 0 1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 0 1 0 0 1
Otorhinolaryngology Lab - LIM32, University of Sao Paulo School of Medicine Clinics Hospital 1 0 0 0 0 1
Clinical Genomics Laboratory, Stanford Medicine 0 1 0 0 0 1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center 0 0 1 0 0 1
New York Genome Center 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 0 1
Institute of Immunology and Genetics Kaiserslautern 0 1 0 0 0 1
MVZ Medizinische Genetik Mainz 0 1 0 0 0 1

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