ClinVar Miner

Variants studied for Weill-Marchesani syndrome 4

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
5 0 227 30 96 356

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic uncertain significance likely benign benign total
ADAMTS17 5 227 30 96 356

Submitter and significance breakdown #

Total submitters: 6
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Submitter pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 223 30 89 341
Nilou-Genome Lab 0 0 0 18 18
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 10 10
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 6 0 0 6
OMIM 5 0 0 0 5
Baylor Genetics 0 1 0 0 1

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