ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.-86T>C

dbSNP: rs886048237
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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 RCV000360499 SCV000371548 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000403401 SCV000371549 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000306906 SCV000371550 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000363760 SCV000371551 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing

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