ClinVar Miner

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

gnomAD frequency: 0.00001  dbSNP: rs961309280
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Total submissions: 3
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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; 11p partial monosomy syndrome 2022-12-06 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
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001530026 SCV001932142 likely benign not provided no assertion criteria provided clinical testing

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