ClinVar Miner

Variants studied for autosomal recessive nonsyndromic hearing loss 31

Included ClinVar conditions (2):
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 not provided total
4 0 120 7 17 1 148

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign not provided total
WHRN 4 120 7 17 1 148

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic uncertain significance likely benign benign not provided total
Illumina Laboratory Services, Illumina 0 107 6 13 0 126
Fulgent Genetics, Fulgent Genetics 1 10 1 0 0 12
Genome-Nilou Lab 0 0 0 11 0 11
Division of Human Genetics, Children's Hospital of Philadelphia 0 3 0 0 0 3
OMIM 2 0 0 0 0 2
Baylor Genetics 0 2 0 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 0 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 0 1
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 1 1

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