ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.29C>A (p.Ala10Asp)

dbSNP: rs997104313
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709155 SCV000838446 uncertain significance Wilms tumor 1 2018-07-02 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002259013 SCV002530528 uncertain significance Hereditary cancer-predisposing syndrome 2021-04-28 criteria provided, single submitter curation

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