ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.294C>T (p.Ala98=)

dbSNP: rs887998910
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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 RCV001479613 SCV001683917 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-02-20 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256791 SCV002530535 likely benign Hereditary cancer-predisposing syndrome 2021-01-18 criteria provided, single submitter curation

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