ClinVar Miner

Variants studied for Denys-Drash syndrome

Included ClinVar conditions (7):
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
32 9 361 119 28 530

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 total
WT1 26 8 175 73 17 290
LOC107982234, WT1 4 1 186 46 11 238
LOC106707172, LOC107982234, WT1 2 0 0 0 0 2

Submitter and significance breakdown #

Total submitters: 16
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 19 3 284 98 14 418
Illumina Clinical Services Laboratory,Illumina 0 0 79 20 12 111
Mendelics 3 1 6 3 1 14
OMIM 13 0 0 0 0 13
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 2 1 5 0 0 8
Athena Diagnostics Inc 0 0 0 0 3 3
Human Genetics Disease in Children – Taif University,Taif University 1 0 0 0 2 3
Fulgent Genetics,Fulgent Genetics 1 0 1 0 0 2
Molecular Diagnostics Laboratory, M Health: University of Minnesota 1 1 0 0 0 2
Human Developmental Genetics,Institut Pasteur 2 0 0 0 0 2
Institute of Human Genetics,Klinikum rechts der Isar 0 1 0 0 0 1
Centre for Translational Omics - GOSgene,University College London 0 1 0 0 0 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 1 0 0 0 1
Institute of Human Genetics, University of Leipzig Medical Center 0 0 1 0 0 1
Broad Institute Rare Disease Group,Broad Institute 1 0 0 0 0 1
Johns Hopkins Genomics,Johns Hopkins University 1 0 0 0 0 1

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