ClinVar Miner

Variants studied for autosomal recessive nonsyndromic deafness 18A

Included ClinVar conditions (3):
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
10 33 66 13 0 119

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
USH1C 10 33 66 13 119

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
Counsyl 5 29 65 13 112
OMIM 2 0 0 0 2
Baylor Genetics 0 0 2 0 2
Fulgent Genetics,Fulgent Genetics 2 0 0 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 1 1 0 0 2
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery,Institute of Otolaryngology, Chinese PLA General Hospital 1 1 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 0 0 1
Division of Human Genetics,Children's Hospital of Philadelphia 0 1 0 0 1

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