ClinVar Miner

Variants studied for Deafness, autosomal recessive 111

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
4 2 0 0 0 5

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic total
MPZL2 4 2 5

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic likely pathogenic total
Laboratory of Molecular Genetics,Brain Korea 21 PLUS Project for Medical Sciences, Yonsei University College of Medicine 3 0 3
OMIM 2 0 2
Baylor Genetics 1 0 1
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 0 1 1
Genetics and Prenatal Diagnosis Center,The First Affiliated Hospital of Zhengzhou University 1 0 1
Neurogenetic Laboratory,Second Faculty of Medicine, Charles University 0 1 1

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