ClinVar Miner

Variants studied for autosomal recessive nonsyndromic deafness 15

Included ClinVar conditions (1):
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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
7 1 3 1 0 12

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
GIPC3 7 1 3 1 12

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
OMIM 6 0 0 0 6
Baylor Genetics 0 0 1 0 1
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 0 0 0 1 1
Fulgent Genetics,Fulgent Genetics 0 0 1 0 1
Hereditary Hearing Loss Research Unit,University of Madras 0 0 1 0 1
The Raphael Recanati Genetics Institute,Rabin Medical Center 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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