ClinVar Miner

Variants studied for Wilms tumor type 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
51 1 239 88 49 426

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 total
GPC3 10 1 77 26 32 146
WT1 12 0 58 40 7 116
LOC107982234, WT1 6 0 70 22 9 106
BRCA2 22 0 33 0 1 56
LOC106707172, LOC107982234, WT1 1 0 0 0 0 1
MED12 0 0 1 0 0 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 21 1 193 87 45 347
Fulgent Genetics 21 0 34 0 1 56
Mendelics 2 0 17 1 0 20
OMIM 9 0 0 0 0 9
Athena Diagnostics Inc 0 0 0 0 3 3
Division of Genomic Diagnostics,The 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
Laboratoire de Cytogenetique,Hospices Civils de Lyon 0 0 1 0 0 1

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