ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.887+19C>G

gnomAD frequency: 0.00001  dbSNP: rs755113185
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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 RCV001949784 SCV002203295 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-03-24 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507596 SCV002815718 uncertain significance Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome 2022-02-14 criteria provided, single submitter clinical testing

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