ClinVar Miner

Variants studied for Epilepsy, childhood absence, susceptibility to, 5

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
1 4 2 0 0 3 9

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
GABRB3 1 4 2 3 9

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance risk factor total
OMIM 0 0 0 3 3
Mendelics 1 1 0 0 2
Baylor Genetics 0 1 0 0 1
Genetic Services Laboratory, University of Chicago 0 1 0 0 1
Mayo Clinic Laboratories, Mayo Clinic 0 0 1 0 1
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille 0 1 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 1

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