Variants studied for Glaucoma 1, open angle, A

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
17	4	38	7	11	73

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
MYOC	17	4	38	7	11	73

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	32	4	11	47
OMIM	15	0	0	0	0	15
Genetics and Molecular Pathology, SA Pathology	2	0	4	0	0	6
Fulgent Genetics, Fulgent Genetics	0	0	0	4	0	4
Revvity Omics, Revvity	0	2	0	0	0	2
Reproductive Health Research and Development, BGI Genomics	2	0	0	0	0	2
Baylor Genetics	1	0	0	0	0	1
Mendelics	1	0	0	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	1	0	0	0	1
Pediatric Genomics Discovery Program, Yale University	0	0	1	0	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	0	0	1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	0	1	0	0	0	1
Pars Genome Lab	0	0	0	1	0	1
3billion	1	0	0	0	0	1
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine	0	0	1	0	0	1

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