ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.333G>T (p.Leu111=)

gnomAD frequency: 0.00001  dbSNP: rs1853459139
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002153384 SCV002458574 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2021-10-08 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002264471 SCV002544556 likely benign not provided 2022-04-01 criteria provided, single submitter clinical testing WT1: BP4, BP7

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