ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.250C>T (p.Leu84=)

dbSNP: rs756055892
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Human Developmental Genetics, Institut Pasteur RCV001257278 SCV001433824 pathogenic Nephrotic syndrome, type 4 2020-04-01 criteria provided, single submitter research
Labcorp Genetics (formerly Invitae), Labcorp RCV003770342 SCV004588273 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-08-08 criteria provided, single submitter clinical testing

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