ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.66G>T (p.Thr22=)

dbSNP: rs1214646426
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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 RCV002076838 SCV002322976 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-07-16 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258362 SCV002530546 uncertain significance Hereditary cancer-predisposing syndrome 2021-12-22 criteria provided, single submitter curation

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