ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.876G>A (p.Thr292=)

dbSNP: rs1343218741
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001475547 SCV001679740 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-10-10 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004007133 SCV004823207 likely benign Wilms tumor 1 2022-11-30 criteria provided, single submitter clinical testing

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