ClinVar Miner

Variants in gene combination LOC107982234, WT1

See also:
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 drug response total
10 3 241 84 13 1 333

Condition and significance breakdown #

Total conditions: 15
Download table as spreadsheet
Condition pathogenic likely pathogenic uncertain significance likely benign benign drug response total
Drash syndrome; Frasier syndrome; Wilms tumor 1; Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 4 1 203 69 8 0 285
Wilms tumor 1 3 0 35 3 5 0 46
Nephrotic syndrome, type 4 2 0 33 4 3 0 42
Meacham syndrome 0 0 28 4 6 0 38
not provided 1 0 5 21 4 0 31
Nephroblastoma 0 0 9 0 0 0 9
Drash syndrome 1 1 5 0 1 0 8
Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 0 0 8 0 0 0 8
not specified 0 0 0 3 6 0 8
Drash syndrome; Frasier syndrome; Nephrotic syndrome, type 4; Wilms tumor 1 0 0 0 0 2 0 2
Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 0 0 1 0 0 0 1
Chronic kidney disease 0 0 1 0 0 0 1
Corticosteroid response 0 0 0 0 0 1 1
Pre-B-cell acute lymphoblastic leukemia 0 1 0 0 0 0 1
none provided 0 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 23
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign drug response total
Invitae 4 1 203 76 8 0 292
Illumina Clinical Services Laboratory,Illumina 0 0 31 7 6 0 38
Mendelics 1 0 14 0 1 0 16
GeneDx 1 0 1 4 4 0 10
PreventionGenetics, PreventionGenetics 0 0 0 1 6 0 7
CeGaT Praxis fuer Humangenetik Tuebingen 0 0 3 2 0 0 5
Integrated Genetics/Laboratory Corporation of America 0 0 0 0 4 0 4
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics 0 0 0 0 4 0 4
Baylor Genetics 0 0 2 0 0 0 2
Athena Diagnostics Inc 0 0 0 0 2 0 2
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories 0 0 0 0 2 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 0 0 2 0 0 0 2
St. Jude Clinical Genomics Lab, St. Jude Children's Research Hospital 0 1 1 0 0 0 2
Human Developmental Genetics,Institut Pasteur 2 0 0 0 0 0 2
OMIM 1 0 0 0 0 0 1
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
Fulgent Genetics,Fulgent Genetics 0 0 1 0 0 0 1
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 0 0 1 0 0 0 1
Institute of Human Genetics, Klinikum rechts der Isar 0 1 0 0 0 0 1
Genetic Testing Lab, Ashok and Rita Patel Institute of Integrated Study and Research in Biotechnology and Allied Sciences 0 0 0 0 0 1 1
Gharavi Laboratory,Columbia University 0 0 1 0 0 0 1
Cavalleri Lab, Royal College of Surgeons in Ireland 0 0 1 0 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.