ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.273G>A (p.Leu91=)

gnomAD frequency: 0.00003  dbSNP: rs1396104394
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001220883 SCV001392896 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-08-08 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258165 SCV002530534 uncertain significance Hereditary cancer-predisposing syndrome 2021-07-22 criteria provided, single submitter curation

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