ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.247G>T (p.Ala83Ser)

dbSNP: rs886048231
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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 RCV000377859 SCV000371500 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000283305 SCV000371501 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000343026 SCV000371502 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000406586 SCV000371503 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing

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