ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.682G>T (p.Asp228Tyr)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005050110 SCV005682760 uncertain significance Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1 2024-03-11 criteria provided, single submitter clinical testing

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