ClinVar Miner

Variants studied for Epilepsy, idiopathic generalized, susceptibility to, 15

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 risk factor total
6 4 6 0 0 4 20

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance risk factor total
RORB 6 4 6 4 20

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic likely pathogenic uncertain significance risk factor total
OMIM 0 0 0 4 4
Institute of Human Genetics, University of Leipzig Medical Center 1 0 1 0 2
3billion 0 1 1 0 2
Baylor Genetics 0 0 1 0 1
Institute of Human Genetics, Cologne University 1 0 0 0 1
MGZ Medical Genetics Center 0 1 0 0 1
Mendelics 1 0 0 0 1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 0 0 1 0 1
Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München 1 0 0 0 1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology 0 1 0 0 1
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics 1 0 0 0 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 0 1 0 1
Génétique des Maladies du Développement, Hospices Civils de Lyon 0 1 0 0 1
New York Genome Center 0 0 1 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 1 0 0 0 1

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