ClinVar Miner

Variants studied for Intellectual disability, X-linked 90

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
9 5 21 0 1 35

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
DLG3 9 5 21 1 35

Submitter and significance breakdown #

Total submitters: 22
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Submitter pathogenic likely pathogenic uncertain significance benign total
Revvity Omics, Revvity 1 0 6 0 7
OMIM 6 0 0 0 6
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 3 0 0 3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 3 0 3
Baylor Genetics 0 0 2 0 2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 1
Fulgent Genetics, Fulgent Genetics 1 0 0 0 1
Strand Center for Genomics and Personalized Medicine, Strand Life Sciences Pvt Ltd 0 0 1 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 1 0 0 1
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 0 0 1 0 1
Medical Genetic Institute of Henan Province, Henan Provincial People’s Hospital 0 0 0 1 1
Reutter Lab, Institute of Human Genetics, University Hospital Bonn 0 0 1 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 1
Neurogenetics Research Program, University of Adelaide 1 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 0 1 0 1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 0 0 1 0 1
Laboratory of Medical Genetics, University of Torino 0 0 1 0 1
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine 0 1 0 0 1
New York Genome Center 0 0 1 0 1
Molecular Genetics Lab, CHRU Brest 0 0 1 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 1
Department of Human Genetics, Hannover Medical School 0 0 1 0 1

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