ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.285C>T (p.Gly95=)

dbSNP: rs886048230
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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 RCV000317141 SCV000371496 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000371797 SCV000371497 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000282320 SCV000371498 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000337292 SCV000371499 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing

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