ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*269G>T

dbSNP: rs886048225
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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 RCV000357375 SCV000371388 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000260222 SCV000371389 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000317710 SCV000371390 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000378547 SCV000371391 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing

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