ClinVar Miner

Variants studied for Deafness, autosomal recessive 49

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
5 3 45 0 2 52

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
MARVELD2 5 3 45 2 52

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance benign total
Illumina Clinical Services Laboratory,Illumina 1 0 43 2 46
OMIM 4 0 0 0 4
Fulgent Genetics,Fulgent Genetics 0 0 2 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 0 1 0 1
UNC Molecular Genetics Laboratory,University of North Carolina at Chapel Hill 0 1 0 0 1
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery,Institute of Otolaryngology, Chinese PLA General Hospital 0 1 0 0 1

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