ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.195G>A (p.Gly65=)

gnomAD frequency: 0.00001  dbSNP: rs1439699290
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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 RCV000861843 SCV001002253 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-09-05 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256563 SCV002530531 likely benign Hereditary cancer-predisposing syndrome 2022-02-07 criteria provided, single submitter curation

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