ClinVar Miner

Variants in gene WDR13

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 25 7 2 32

Condition and significance breakdown #

Total conditions: 3
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Condition uncertain significance likely benign benign total
not specified 23 0 0 23
not provided 4 7 2 12
Esophageal atresia; Pyloric stenosis 1 0 0 1

Submitter and significance breakdown #

Total submitters: 9
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Submitter uncertain significance likely benign benign total
Ambry Genetics 23 0 0 23
Labcorp Genetics (formerly Invitae), Labcorp 0 3 2 5
CeGaT Center for Human Genetics Tuebingen 0 4 0 4
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 3 1 0 4
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ 2 0 0 2
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) 1 1 0 2
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center 1 0 0 1
Clinical Genetics, Erasmus University Medical Center 1 0 0 1
Breakthrough Genomics, Breakthrough Genomics 0 0 1 1

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