ClinVar Miner

Variants studied for autosomal recessive nonsyndromic deafness 21

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
7 0 132 8 8 155

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
TBCEL-TECTA, TECTA 7 132 8 8 155

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 130 8 8 146
National Institute on Deafness and Communication Disorders,National Institutes of Health 3 0 0 0 3
Fulgent Genetics,Fulgent Genetics 0 1 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 1 0 0 1
Laboratory of Prof. Karen Avraham,Tel Aviv University 1 0 0 0 1
Hereditary Research Laboratory, Bethlehem University 1 0 0 0 1
Laboratory of NeuroGenetics and Regenerative Medicine,University of Maryland School of Medicine 1 0 0 0 1
Genomic Medicine Lab, University of California San Francisco 0 1 0 0 1
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery,Institute of Otolaryngology, Chinese PLA General Hospital 1 0 0 0 1

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