ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.662-5C>T

gnomAD frequency: 0.00001  dbSNP: rs780259089
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000542648 SCV000657633 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2024-01-12 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256395 SCV002530549 uncertain significance Hereditary cancer-predisposing syndrome 2022-02-09 criteria provided, single submitter curation
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316729 SCV004016270 likely benign Wilms tumor 1 2023-07-07 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707347 SCV005224183 likely benign not provided criteria provided, single submitter not provided

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