ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*393G>T

dbSNP: rs886048222
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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 RCV000280600 SCV000371372 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000319262 SCV000371373 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000371566 SCV000371374 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000286056 SCV000371375 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing

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