ClinVar Miner

List of variants reported as likely benign for Nephrotic syndrome, type 4 by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 20
Download table as spreadsheet
NM_024426.6(WT1):c.*1098C>T rs5030327
NM_024426.6(WT1):c.*1132A>T rs5030328
NM_024426.6(WT1):c.*1209A>G rs5030329
NM_024426.6(WT1):c.*1239T>A rs534396876
NM_024426.6(WT1):c.*138G>A rs111351882
NM_024426.6(WT1):c.*16G>T rs2234594
NM_024426.6(WT1):c.*345G>A rs5030318
NM_024426.6(WT1):c.*542G>A rs142726499
NM_024426.6(WT1):c.*835A>G rs5030322
NM_024426.6(WT1):c.*864T>A rs5030323
NM_024426.6(WT1):c.*864T>G rs5030323
NM_024426.6(WT1):c.*897G>C rs5030324
NM_024426.6(WT1):c.*903G>A rs5030325
NM_024426.6(WT1):c.1114-9T>C rs5030274
NM_024426.6(WT1):c.1154G>A (p.Arg385Gln) rs147241955
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661
NM_024426.6(WT1):c.181C>A (p.Arg61=) rs2234581
NM_024426.6(WT1):c.216G>T (p.Gln72His) rs5030135
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682
NM_024426.6(WT1):c.760C>T (p.Pro254Ser) rs2234584

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.