ClinVar Miner

Variants studied for Wilms tumor 1

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 not provided total
60 13 507 304 99 3 978

Gene and significance breakdown #

Total genes and gene combinations: 6
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
GPC3 41 6 427 289 69 0 830
WT1 12 4 33 11 22 3 83
LOC107982234, WT1 4 3 38 4 8 0 53
TRIM28 0 0 6 0 0 0 6
BRCA2 3 0 1 0 0 0 4
LOC130065239, TRIM28 0 0 2 0 0 0 2

Submitter and significance breakdown #

Total submitters: 20
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Invitae 39 6 425 289 69 0 828
Illumina Laboratory Services, Illumina 0 0 48 11 23 0 82
Mendelics 2 0 17 1 1 0 21
Genome-Nilou Lab 0 0 0 0 18 0 18
St. Jude Molecular Pathology, St. Jude Children's Research Hospital 3 0 14 0 0 0 17
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 3 10 0 13
Baylor Genetics 4 2 4 0 0 0 10
OMIM 9 0 0 0 0 0 9
GeneReviews 0 0 0 0 0 3 3
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 0 1 1 0 0 0 2
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 2 0 0 0 2
Genetics and Molecular Pathology, SA Pathology 1 1 0 0 0 0 2
Institute of Human Genetics, Clinical Exome/Genome Diagnostics Group, University Hospital Bonn 2 0 0 0 0 0 2
Molecular Genetics and NGS Laboratory, Hospital Fundacion Valle Del Lili 1 1 0 0 0 0 2
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia 0 0 0 1 0 0 1
Institute of Human Genetics, Cologne University 1 0 0 0 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 0 0 1
Institute for Human Genetics and Genomic Medicine, Uniklinik RWTH Aachen 0 1 0 0 0 0 1
Donald Williams Parsons Laboratory, Baylor College of Medicine 1 0 0 0 0 0 1
Laan Lab, Human Genetics Research Group, University of Tartu 0 1 0 0 0 0 1

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