ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.45G>A (p.Pro15=)

dbSNP: rs1158182061
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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 RCV000802455 SCV000942287 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2022-11-08 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004803231 SCV005428497 likely benign Wilms tumor 1 2024-05-14 criteria provided, single submitter clinical testing

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