ClinVar Miner

Variants studied for Deafness, autosomal dominant 56

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
2 0 9 1 0 12

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign total
TNC 2 8 1 11

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic uncertain significance likely benign total
Baylor Genetics 0 4 0 4
OMIM 2 0 0 2
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 2 0 2
Institute of Human Genetics, University of Leipzig Medical Center 0 1 0 1
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 0 1 0 1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 0 1 0 1
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery,Institute of Otolaryngology, Chinese PLA General Hospital 0 0 1 1

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