ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.136G>T (p.Ala46Ser)

dbSNP: rs886048233
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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 RCV000292853 SCV000371524 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000352305 SCV000371525 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000405576 SCV000371526 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000299099 SCV000371527 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing

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