ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*1058G>T (rs886048211)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000377414 SCV000371248 uncertain significance Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000285242 SCV000371249 uncertain significance Wilms Tumor 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000342608 SCV000371250 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000371485 SCV000371251 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing

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