ClinVar Miner

Variants in gene GRID2

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 not provided total
17 11 131 85 50 1 280

Condition and significance breakdown #

Total conditions: 8
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Condition pathogenic likely pathogenic uncertain significance likely benign benign not provided total
not provided 4 4 57 77 50 0 183
Inborn genetic diseases 2 0 73 0 0 0 75
Autosomal recessive spinocerebellar ataxia 18 10 3 11 0 2 0 26
See cases 1 2 5 4 0 0 12
GRID2-related disorder 0 0 0 9 2 0 11
Schizophrenia 0 2 0 0 0 0 2
not specified 0 0 2 0 0 0 2
Gestational diabetes mellitus uncontrolled 0 0 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 35
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 2 0 30 65 24 0 121
Ambry Genetics 2 0 73 0 0 0 75
GeneDx 0 3 11 8 29 0 51
Breakthrough Genomics, Breakthrough Genomics 0 0 0 5 20 0 25
CeGaT Center for Human Genetics Tuebingen 0 0 5 6 3 0 14
PreventionGenetics, part of Exact Sciences 0 0 0 9 2 0 11
Quest Diagnostics Nichols Institute San Juan Capistrano 0 0 5 2 0 0 7
ISCA site 1 1 1 3 1 0 0 6
Mayo Clinic Laboratories, Mayo Clinic 0 0 5 0 0 0 5
Institute of Human Genetics, University of Leipzig Medical Center 1 0 4 0 0 0 5
OMIM 4 0 0 0 0 0 4
Baylor Genetics 0 0 3 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 1 1 0 0 0 3
Bionano Laboratories 2 0 1 0 0 0 3
Department of Psychiatry, Nagoya University 0 2 0 0 0 0 2
Genome-Nilou Lab 0 0 0 0 2 0 2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 0 1 0 0 0 0 1
Institute of Human Genetics, University of Goettingen 0 0 1 0 0 0 1
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 1 0 0 0 1
ARUP Laboratories, Cytogenetics and Genomic Microarray, ARUP Laboratories 0 0 1 0 0 0 1
Eurofins Ntd Llc (ga) 0 0 1 0 0 0 1
Fulgent Genetics, Fulgent Genetics 0 0 1 0 0 0 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 1 0 0 0 1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 0 1 0 0 0 0 1
Institute of Human Genetics, FAU Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg 1 0 0 0 0 0 1
ISCA site 4 0 0 0 1 0 0 1
Institute of Molecular and Cell Biology, University of Tartu 0 0 0 0 0 1 1
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 1 0 0 0 0 0 1
Research Group Niklas Dahl, Uppsala University 1 0 0 0 0 0 1
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 1 0 0 0 1
Center for Personalized Medicine, Children's Hospital Los Angeles 0 1 0 0 0 0 1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 0 0 1 0 0 0 1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 1 0 0 0 0 1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 1 0 0 0 0 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 0 1 0 0 1

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