ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.472G>T (p.Glu158Ter)

dbSNP: rs1565001383
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000709146 SCV000838437 pathogenic Wilms tumor 1 2018-07-02 criteria provided, single submitter clinical testing
Mendelics RCV000988519 SCV001138267 pathogenic Drash syndrome 2019-05-28 criteria provided, single submitter clinical testing

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