ClinVar Miner

Variants studied for Autosomal recessive nonsyndromic hearing loss 84B

Coded as:
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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 not provided total
13 13 22 0 5 3 53

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign not provided total
OTOGL 13 13 22 5 3 53

Submitter and significance breakdown #

Total submitters: 20
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Submitter pathogenic likely pathogenic uncertain significance benign not provided total
Revvity Omics, Revvity 2 5 4 0 0 11
Fulgent Genetics, Fulgent Genetics 2 3 5 0 0 10
Baylor Genetics 0 0 7 0 0 7
Genome-Nilou Lab 0 0 0 5 0 5
OMIM 3 0 0 0 0 3
GenomeConnect, ClinGen 0 0 0 0 3 3
3billion 3 0 0 0 0 3
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 2 0 0 3
King Laboratory, University of Washington 0 2 0 0 0 2
MGZ Medical Genetics Center 1 1 0 0 0 2
Service de Biologie Medicale, CIUSSS du Saguenay-Lac-Saint-Jean 0 1 1 0 0 2
WangQJ Lab, Chinese People's Liberation Army General Hospital 0 1 1 0 0 2
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 0 0 1 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 0 1 0 0 0 1
Genome Diagnostics Laboratory, Amsterdam University Medical Center 1 0 0 0 0 1
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 1 0 0 0 0 1
Tehran Medical Genetics Laboratory 0 1 0 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 0 1 0 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 1 0 0 0 0 1

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