Variants studied for Intellectual disability, X-linked 106

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
7	4	18	0	0	1	29

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	not provided	total
OGT	7	4	18	1	29

Submitter and significance breakdown #

Total submitters: 18

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Submitter	pathogenic	likely pathogenic	uncertain significance	not provided	total
OMIM	6	0	0	0	6
Baylor Genetics	0	2	4	0	6
Daan van Aalten Lab, University of Dundee	5	0	1	0	6
Revvity Omics, Revvity	0	0	3	0	3
MGZ Medical Genetics Center	0	0	1	0	1
Centogene AG - the Rare Disease Company	0	0	1	0	1
Randwick Genomics Laboratory, Prince of Wales Hospital Sydney, Australia, New South Wales Health Pathology	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	1
Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München	0	1	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	1	0	1
Illumina Laboratory Services, Illumina	0	0	1	0	1
Medical Genetic Institute of Henan Province, Henan Provincial People’s Hospital	0	0	1	0	1
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	0	1	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	1	0	0	0	1
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill	0	0	1	0	1
GenomeConnect - Brain Gene Registry	0	0	0	1	1

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