ClinVar Miner

Variants studied for Nephroblastoma

Coded as:
Minimum submission review status: Collection method:
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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 other total
4 1 26 5 10 6 52

Gene and significance breakdown #

Total genes and gene combinations: 12
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign other total
WT1 1 0 16 5 5 0 27
LOC107982234, WT1 0 0 9 0 5 0 14
CTNNB1, LOC126806658 0 0 0 0 0 2 2
BRAF 1 0 0 0 0 0 1
CHEK2 1 0 0 0 0 0 1
CTNNB1 0 0 0 0 0 1 1
DIS3L2 0 1 0 0 0 0 1
FZD6 0 0 0 0 0 1 1
MED12 0 0 0 0 0 1 1
SMAD4 0 0 1 0 0 0 1
TET2 0 0 0 0 0 1 1
TRIM28 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign other total
Illumina Laboratory Services, Illumina 0 0 24 3 2 0 29
Color Diagnostics, LLC DBA Color Health 0 0 0 2 8 0 10
Donald Williams Parsons Laboratory, Baylor College of Medicine 1 1 0 0 0 6 8
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 0 0 2 0 0 0 2
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 1 0 0 0 0 0 1
Pediatric Oncology, Johns Hopkins University 1 0 0 0 0 0 1
NPCF Sunshine Lab, H. Lee Moffitt Cancer Center and Research Institute 1 0 0 0 0 0 1

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