ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.468G>T (p.Pro156=) (rs961309280)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000464052 SCV000557453 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome 2020-10-10 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001530026 SCV001744531 likely benign not provided no assertion criteria provided clinical testing

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