ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1275A>G (p.Pro425=)

dbSNP: rs2132921460
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002258418 SCV002530519 likely benign Hereditary cancer-predisposing syndrome 2022-01-09 criteria provided, single submitter curation
Labcorp Genetics (formerly Invitae), Labcorp RCV003101404 SCV003477992 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-06-13 criteria provided, single submitter clinical testing

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