ClinVar Miner

Variants studied for Wilms tumor 1; Simpson-Golabi-Behmel syndrome type 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 total
0 0 12 14 0 26

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination uncertain significance likely benign total
GPC3 11 14 25
MED12 1 0 1

Submitter and significance breakdown #

Total submitters: 2
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Submitter uncertain significance likely benign total
Fulgent Genetics, Fulgent Genetics 11 14 25
Génétique des Maladies du Développement, Hospices Civils de Lyon 1 0 1

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