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
63 17 635 387 103 3 1194

Gene and significance breakdown #

Total genes and gene combinations: 7
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
GPC3 43 8 428 289 69 0 835
WT1 12 6 86 54 25 3 178
LOC107982234, WT1 4 3 112 44 9 0 168
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
CCDC160, GPC3, HPRT1, MIR106A, MIR19B2, PHF6 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 22
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 42 8 426 289 69 0 834
All of Us Research Program, National Institutes of Health 0 2 139 84 4 0 229
Illumina Laboratory Services, Illumina 0 0 48 11 23 0 82
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
Mendelics 0 0 11 0 1 0 12
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
MVZ Medizinische Genetik Mainz 1 0 0 0 0 0 1

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