ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.1448-10G>T

dbSNP: rs185744719
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000872698 SCV001014551 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-11-18 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001811527 SCV001471648 likely benign not provided 2020-08-27 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004549966 SCV004721572 likely benign WT1-related disorder 2023-01-26 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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