ClinVar Miner

Variants studied for Deafness, autosomal recessive 22

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
6 4 9 0 2 21

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
OTOA 6 4 9 2 21

Submitter and significance breakdown #

Total submitters: 14
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 4 0 0 0 4
Fulgent Genetics,Fulgent Genetics 0 0 3 0 3
Baylor Genetics 0 1 1 0 2
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 0 0 0 2 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 2 0 2
Mendelics 1 0 0 0 1
Victorian Clinical Genetics Services,Murdoch Childrens Research Institute 0 0 1 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 0 1 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 1 0 0 1
Baylor-Hopkins Center for Mendelian Genomics,Johns Hopkins University 0 0 1 0 1
Hereditary Research Laboratory, Bethlehem University 1 0 0 0 1
Santos-Cortez Lab,University of Colorado School of Medicine 0 1 0 0 1
Laboratory of Molecular Genetics,Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine 1 0 0 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 0 1 0 0 1

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