ClinVar Miner

Variants studied for Wilms tumor 1

Included ClinVar conditions (8):
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
78 10 652 275 94 1088

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 total
GPC3 24 4 205 98 56 386
WT1 22 5 187 105 26 334
LOC107982234, WT1 7 1 225 72 11 307
BRCA2 22 0 34 0 1 57
LOC106707172, LOC107982234, WT1 2 0 0 0 0 2
DCDC1, DNAJC24, ELP4, IMMP1L, PAX6, RCN1, WT1 1 0 0 0 0 1
MED12 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 16
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 47 9 568 264 74 962
Illumina Clinical Services Laboratory,Illumina 0 0 48 11 23 82
Fulgent Genetics,Fulgent Genetics 21 0 34 0 1 56
Mendelics 2 0 17 1 1 21
OMIM 9 0 0 0 0 9
Baylor Genetics 0 0 3 0 0 3
Athena Diagnostics Inc 0 0 0 0 3 3
GeneReviews 3 0 0 0 0 3
Human Genome Sequencing Center Clinical Lab, Baylor College of Medicine 0 1 1 0 0 2
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 2 0 0 2
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics,Children's Hospital of Philadelphia 0 0 0 1 0 1
Institute of Human Genetics,Cologne University 1 0 0 0 0 1
Donald Williams Parsons Laboratory,Baylor College of Medicine 1 0 0 0 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 1
Génétique des Maladies du Développement, Hospices Civils de Lyon 0 0 1 0 0 1
Johns Hopkins Genomics, Johns Hopkins University 1 0 0 0 0 1

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