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
24 3 170 86 23 295

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 20 3 87 59 13 179
LOC107982234, WT1 3 0 83 27 10 115
LOC106707172, LOC107982234, WT1 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 13 0 116 61 13 203
Illumina Clinical Services Laboratory,Illumina 0 0 56 25 7 88
OMIM 13 0 0 0 0 13
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 2 1 3 0 0 6
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 1 0 1 0 0 2
Molecular Diagnostics Laboratory,M Health: University of Minnesota 1 1 0 0 0 2
Centre for Translational Omics - GOSgene,University College London 0 1 0 0 0 1
Broad Institute Rare Disease Group,Broad Institute 1 0 0 0 0 1

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