ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.-90T>C

dbSNP: rs886048238
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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 RCV000271498 SCV000371552 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000328926 SCV000371553 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000367318 SCV000371554 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000275075 SCV000371555 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing

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