ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1448-10G>A

dbSNP: rs185744719
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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 RCV000464731 SCV000557445 benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2024-01-18 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256290 SCV002530524 benign Hereditary cancer-predisposing syndrome 2021-12-23 criteria provided, single submitter curation
Fulgent Genetics, Fulgent Genetics RCV002496811 SCV002807950 likely benign Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome 2021-10-22 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004002125 SCV004824841 benign Wilms tumor 1 2023-12-13 criteria provided, single submitter clinical testing

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