ClinVar Miner

Variants studied for Autosomal dominant nonsyndromic deafness 17

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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
3 0 115 49 35 202

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
MYH9 3 115 49 35 202

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 113 48 35 196
OMIM 1 0 0 0 1
Baylor Genetics 0 1 0 0 1
Clinical Genetics laboratory, University of Goettingen 0 0 1 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 1 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 1 0 0 0 1
Genomics England Pilot Project,Genomics England 1 0 0 0 1

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