ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.*542G>A

gnomAD frequency: 0.00380  dbSNP: rs142726499
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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 RCV000338201 SCV000371356 likely benign Nephroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000406182 SCV000371357 likely benign 11p partial monosomy syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000298577 SCV000371358 likely benign Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000334858 SCV000371359 likely benign Nephrotic syndrome, type 4 2016-06-14 criteria provided, single submitter clinical testing

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