ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.315G>T (p.Ala105=)

dbSNP: rs1554946607
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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 RCV002116768 SCV002390099 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2021-12-24 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258378 SCV002530539 likely benign Hereditary cancer-predisposing syndrome 2020-10-13 criteria provided, single submitter curation

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