ClinVar Miner

Submissions for variant NM_024426.6(WT1):c.115C>A (p.Arg39=)

gnomAD frequency: 0.00001  dbSNP: rs763147828
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000876473 SCV001019049 likely benign Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome 2023-07-17 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258021 SCV002530510 likely benign Hereditary cancer-predisposing syndrome 2021-03-22 criteria provided, single submitter curation
Fulgent Genetics, Fulgent Genetics RCV002478992 SCV002799842 likely benign Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome 2021-08-31 criteria provided, single submitter clinical testing

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.