ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1016+15C>T

gnomAD frequency: 0.00004  dbSNP: rs752756426
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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 RCV002078197 SCV002373483 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-12-08 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507938 SCV002797991 likely benign Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome 2021-09-28 criteria provided, single submitter clinical testing

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