ClinVar Miner

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

dbSNP: 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 Laboratory Services, Illumina RCV000377414 SCV000371248 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000285242 SCV000371249 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000342608 SCV000371250 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000371485 SCV000371251 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing

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