Variants studied for Autosomal recessive nonsyndromic hearing loss 93

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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
2	4	4	1	1	11

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	benign	total
CABP2	2	4	4	1	1	11

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	0	0	2	1	0	3
Revvity Omics, Revvity	1	1	0	0	0	2
Laboratory of Prof. Karen Avraham, Tel Aviv University	2	0	0	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	1	0	1	0	0	2
OMIM	1	0	0	0	0	1
Intergen, Intergen Genetics and Rare Diseases Diagnosis Center	0	1	0	0	0	1
Institute of Human Genetics, University of Ulm	0	1	0	0	0	1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	1	0	0	0	0	1
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine	1	0	0	0	0	1
Center for Statistical Genetics, Columbia University	1	0	0	0	0	1
Daryl Scott Lab, Baylor College of Medicine	0	0	1	0	0	1
Genetics Laboratory, Department of Biology, Semnan University	0	1	0	0	0	1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center	1	0	0	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
Molecular Diagnostics Lab, Aalborg University Hospital	1	0	0	0	0	1

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