ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.513C>A (p.Gly171=) (rs536728682)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000355484 SCV000371468 likely benign Meacham syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000265420 SCV000371469 likely benign Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000320486 SCV000371470 likely benign Wilms Tumor 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000360737 SCV000371471 likely benign Diffuse mesangial sclerosis 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000468659 SCV000557448 benign Drash syndrome; Frasier syndrome; Wilms tumor 1; Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 2017-12-27 criteria provided, single submitter clinical testing
PreventionGenetics RCV000242436 SCV000314315 benign not specified criteria provided, single submitter clinical testing

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