ClinVar Miner

Variants in gene MAG

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
8 7 151 139 28 321

Condition and significance breakdown #

Total conditions: 6
Download table as spreadsheet
Condition pathogenic likely pathogenic uncertain significance likely benign benign total
Hereditary spastic paraplegia 75 8 6 101 127 18 258
Inborn genetic diseases 0 0 67 2 0 69
not provided 0 1 11 17 18 45
MAG-related disorder 0 0 0 11 2 13
not specified 0 0 2 4 1 7
Hereditary spastic paraplegia 0 0 3 0 0 3

Submitter and significance breakdown #

Total submitters: 24
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Labcorp Genetics (formerly Invitae), Labcorp 2 3 96 129 18 248
Ambry Genetics 0 0 67 2 0 69
Breakthrough Genomics, Breakthrough Genomics 0 0 3 5 15 23
CeGaT Center for Human Genetics Tuebingen 0 0 4 12 1 17
GeneDx 0 0 3 0 10 13
PreventionGenetics, part of Exact Sciences 0 0 0 11 2 13
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 1 4 0 6
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 2 1 0 0 0 3
Unit for Genetic & Epidemiological Research on Neurological Disorders, Instituto de Investigação e Inovação em Saúde 0 0 3 0 0 3
OMIM 2 0 0 0 0 2
Baylor Genetics 0 0 2 0 0 2
Mayo Clinic Laboratories, Mayo Clinic 0 0 2 0 0 2
Genome-Nilou Lab 0 0 0 0 2 2
Genetic Services Laboratory, University of Chicago 0 1 0 0 0 1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia 0 0 0 0 1 1
Fulgent Genetics, Fulgent Genetics 0 0 0 1 0 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics 0 0 1 0 0 1
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 1 0 0 1
Kariminejad - Najmabadi Pathology & Genetics Center 0 0 1 0 0 1
New York Genome Center 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 1 0 0 0 1
Solve-RD Consortium 0 1 0 0 0 1
Medical Genetics Laboratory, AJA University of Medical Sciences 1 0 0 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.