Variants studied for Wagner disease

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	not provided	total
9	1	87	79	76	11	251

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	not provided	total
VCAN	9	1	87	79	76	11	251

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Illumina Laboratory Services, Illumina	0	0	78	76	74	0	228
GeneReviews	0	0	0	0	0	11	11
Genome-Nilou Lab	0	0	0	0	11	0	11
OMIM	8	0	0	0	0	0	8
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	2	0	2	0	4
Fulgent Genetics, Fulgent Genetics	0	0	2	2	0	0	4
Genome Diagnostics Laboratory, Amsterdam University Medical Center	0	0	0	0	4	0	4
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	0	0	0	4	0	0	4
Revvity Omics, Revvity	0	0	3	0	0	0	3
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	2	0	0	0	2
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	0	0	0	0	2	0	2
Molecular Genetics Laboratory, Institute for Ophthalmic Research	1	0	0	0	0	0	1
Mendelics	0	1	0	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	0	1
Al Jalila Children's Genomics Center, Al Jalila Childrens Speciality Hospital	0	0	0	0	1	0	1
3billion	1	0	0	0	0	0	1

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