Variants studied for Neurodevelopmental disorder with absent language and variable seizures

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
6	1	7	0	0	14

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
WASF1	6	1	7	14

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
OMIM	3	0	0	3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	2	0	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	2	0	0	2
Fulgent Genetics, Fulgent Genetics	0	0	2	2
Revvity Omics, Revvity	0	0	1	1
MGZ Medical Genetics Center	0	0	1	1
Clinical Genomics Laboratory, Washington University in St. Louis	0	0	1	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	1	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	1	0	0	1
Institute of Human Genetics, Heidelberg University	1	0	0	1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	0	0	1	1
New York Genome Center	0	1	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	1
Department of Rehabilitation, Children’s Hospital of Chongqing Medical University	1	0	0	1

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