ClinVar Miner

Variants studied for developmental and epileptic encephalopathy, 34

Included ClinVar conditions (2):
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
33 14 314 482 30 11 871

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
SLC12A5 33 13 305 470 30 11 849
LOC113960611, SLC12A5 0 1 7 12 0 0 20
LOC130065980, SLC12A5 0 0 2 0 0 0 2

Submitter and significance breakdown #

Total submitters: 18
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 29 8 297 482 29 0 845
GeneReviews 0 0 0 0 0 11 11
Baylor Genetics 0 0 9 0 0 0 9
Revvity Omics, Revvity 1 1 5 0 0 0 7
Fulgent Genetics, Fulgent Genetics 0 0 7 0 0 0 7
New York Genome Center 0 0 6 0 0 0 6
OMIM 3 0 0 0 0 0 3
Genome-Nilou Lab 0 0 0 0 3 0 3
Centre for Inherited Metabolic Diseases, Karolinska University Hospital 0 2 0 0 0 0 2
Institute for Medical Genetics and Human Genetics, Charité - Universitätsmedizin Berlin 1 1 0 0 0 0 2
Laboratory of Medical Genetics, National & Kapodistrian University of Athens 0 2 0 0 0 0 2
Mendelics 0 0 0 0 1 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 0 1
NeuroMeGen, Hospital Clinico Santiago de Compostela 0 1 0 0 0 0 1
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 1 0 0 0 1
Daryl Scott Lab, Baylor College of Medicine 0 0 1 0 0 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 0 1
3billion, Medical Genetics 0 0 1 0 0 0 1

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