ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*1021GT[19]

dbSNP: rs58549495
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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 RCV000279212 SCV000371252 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000336733 SCV000371253 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000394767 SCV000371254 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000311367 SCV000371255 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing

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