ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*1021GT[18]

dbSNP: rs58549495
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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000311035 SCV000371264 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000350607 SCV000371265 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000268186 SCV000371266 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000316345 SCV000371267 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000350607 SCV000371276 uncertain significance Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000268186 SCV000371277 uncertain significance 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000311035 SCV000371278 uncertain significance Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000316345 SCV000371279 uncertain significance Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004693032 SCV005191240 uncertain significance not provided criteria provided, single submitter not provided

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