ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1059C>T (p.Ile353=)

gnomAD frequency: 0.00005  dbSNP: rs527655625
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000288082 SCV000345343 uncertain significance not provided 2016-09-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001081282 SCV000557449 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2024-01-04 criteria provided, single submitter clinical testing

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