ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.810C>A (p.Pro270=)

gnomAD frequency: 0.00001  dbSNP: rs1357760274
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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 RCV000864549 SCV001005361 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2024-08-31 criteria provided, single submitter clinical testing

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