ClinVar Miner

Variants studied for Autosomal dominant nonsyndromic hearing loss 10

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
12 16 62 11 24 124

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
EYA4, TARID 4 5 42 7 15 73
EYA4 8 10 19 4 9 49
EYA4, LOC126859796, TARID 0 1 1 0 0 2

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 0 58 11 24 93
Institute of Rare Diseases, West China Hospital, Sichuan University 0 8 0 0 0 8
OMIM 4 0 0 0 0 4
Laboratory of Prof. Karen Avraham, Tel Aviv University 3 1 0 0 0 4
Genome-Nilou Lab 1 0 0 0 2 3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 2 0 0 2
3billion 0 1 1 0 0 2
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital 2 0 0 0 0 2
King Laboratory, University of Washington 1 0 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 0 0 1
Santos-Cortez Lab, University of Colorado School of Medicine 0 1 0 0 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 0 1 0 0 0 1
Clinical Genomics Laboratory, Stanford Medicine 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 1 0 0 0 1
WangQJ Lab, Chinese People's Liberation Army General Hospital 1 0 0 0 0 1
MVZ Medizinische Genetik Mainz 0 1 0 0 0 1
Otorhinolaryngology Head and Neck Surgery, First Medical Center of Chinese PLA General Hospital 0 1 0 0 0 1

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