Variants studied for Van Maldergem syndrome 2

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
8	1	19	0	15	43

Gene and significance breakdown #

Total genes and gene combinations: 1

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
FAT4	8	1	19	15	43

Submitter and significance breakdown #

Total submitters: 15

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Genome-Nilou Lab	0	0	0	15	15
OMIM	6	0	0	0	6
Baylor Genetics	0	0	4	0	4
Mendelics	0	0	1	2	3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	3	0	3
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	0	3	0	3
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	2	0	2
Undiagnosed Diseases Network, NIH	0	0	2	0	2
UNC Molecular Genetics Laboratory, University of North Carolina at Chapel Hill	0	0	2	0	2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	0	1	0	0	1
Clinical Genomics Laboratory, Washington University in St. Louis	0	0	1	0	1
Department of Medical Genetics and Molecular Biology, School of Medicine, Iran University of Medical Sciences	1	0	0	0	1
Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University	1	0	0	0	1
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine	0	0	1	0	1
Al Jawhara Center for Molecular Medicine, Arabian Gulf University	0	0	1	0	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.