ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.153C>T (p.Ala51=)

dbSNP: rs1590411186
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000924163 SCV001069670 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2024-01-05 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002259052 SCV002530522 likely benign Hereditary cancer-predisposing syndrome 2021-08-26 criteria provided, single submitter curation

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