ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.780G>A (p.Ser260=)

dbSNP: rs1403311573
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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 RCV002157240 SCV002334170 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2021-03-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498131 SCV002804783 likely benign Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome 2021-11-30 criteria provided, single submitter clinical testing

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