ClinVar Miner

Variants studied for Mental retardation, X-linked 102

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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
39 17 3 1 0 56

Gene and significance breakdown #

Total genes and gene combinations: 1
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign total
DDX3X 39 17 3 1 56

Submitter and significance breakdown #

Total submitters: 24
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign total
OMIM 13 0 0 0 13
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 6 0 0 6
Molecular Genetics Laboratory,BC Children's and BC Women's Hospitals 3 1 0 0 4
Mendelics 4 0 0 0 4
Institute of Human Genetics,Klinikum rechts der Isar 4 0 0 0 4
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 4 0 0 0 4
Institute of Human Genetics, University of Leipzig Medical Center 0 2 2 0 4
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 3 0 0 0 3
Baylor Genetics 1 1 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 1 1 0 2
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 2 0 0 0 2
Center for Human Genetics,University of Leuven 0 2 0 0 2
Center for Human Genetics and Laboratory Diagnostics, Dr. Klein, Dr. Rost and Colleagues 2 0 0 0 2
Institute for Genomic Medicine (IGM) Clinical Laboratory,Nationwide Children's Hospital 2 0 0 0 2
Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn 2 0 0 0 2
Integrated Genetics/Laboratory Corporation of America 0 1 0 0 1
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 1 0 0 1
Fulgent Genetics,Fulgent Genetics 0 1 0 0 1
Service de Génétique Moléculaire,Hôpital Robert Debré 0 0 0 1 1
Dobyns Lab,Seattle Children's Research Institute 1 0 0 0 1
Undiagnosed Diseases Network,NIH 0 1 0 0 1
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 1 0 0 0 1
Genomic Medicine Lab, University of California San Francisco 1 0 0 0 1
Clinical Genomics Program,Stanford Medicine 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.