ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1011G>A (p.Gln337=)

dbSNP: rs1590373398
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001486650 SCV001691115 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2018-06-06 criteria provided, single submitter clinical testing

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