ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*574del

gnomAD frequency: 0.00007  dbSNP: rs5030319
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000296051 SCV000371352 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000350862 SCV000371353 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000386761 SCV000371354 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000292620 SCV000371355 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing

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