Variants studied for Intellectual developmental disorder with cardiac defects and dysmorphic facies

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	7	19	0	2	34

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
TMEM94	8	7	19	2	34

Submitter and significance breakdown #

Total submitters: 18

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Baylor Genetics	0	0	9	0	9
OMIM	7	0	0	0	7
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	2	0	2
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues	0	0	2	0	2
Genome-Nilou Lab	0	0	0	2	2
3billion	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	2	0	0	2
Department of Human Genetics, Hannover Medical School	0	1	1	0	2
Revvity Omics, Revvity	0	0	1	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	1	0	0	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	0	0	1	0	1
Daryl Scott Lab, Baylor College of Medicine	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	1
Department of Pathology and Laboratory Medicine, Sinai Health System	0	1	0	0	1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	1	0	0	1
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	0	1	0	0	1
New York Genome Center	0	0	1	0	1
Breakthrough Genomics, Breakthrough Genomics	0	1	0	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.