ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1017-11T>C

dbSNP: rs1564975924
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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 RCV002130925 SCV002441918 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-07-26 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258387 SCV002530509 uncertain significance Hereditary cancer-predisposing syndrome 2022-01-18 criteria provided, single submitter curation

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