ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.952G>A (p.Ala318Thr)

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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 RCV005046724 SCV005676076 uncertain significance Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1 2024-05-02 criteria provided, single submitter clinical testing

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