Variants studied for Intellectual developmental disorder, autosomal recessive 71

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
4	5	13	1	5	26

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
ALKBH8	4	5	13	1	5	26

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	2	2	3	0	0	7
Genome-Nilou Lab	0	0	0	0	5	5
OMIM	3	0	0	0	0	3
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	0	2	0	0	2
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	2	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	0	2	0	0	2
New York Genome Center	0	0	2	0	0	2
3billion	0	1	0	0	0	1
Baylor Genetics	0	1	0	0	0	1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS)	1	0	0	0	0	1
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	1	0	0	1
Fulgent Genetics, Fulgent Genetics	0	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	1
University of Washington Department of Laboratory Medicine, University of Washington	0	1	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	1

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