ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as likely benign for Denys-Drash syndrome

Included ClinVar conditions (7):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
NM_024426.6(WT1):c.123G>C (p.Pro41=) rs555140661
NM_024426.6(WT1):c.150C>T (p.Ala50=) rs1554946724
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.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.315G>A (p.Ala105=) rs1554946607
NM_024426.6(WT1):c.381C>T (p.Pro127=) rs771681406
NM_024426.6(WT1):c.42C>T (p.Val14=) rs1343194102
NM_024426.6(WT1):c.450C>T (p.Ser150=) rs1213710686
NM_024426.6(WT1):c.480G>A (p.Gln160=) rs758900425
NM_024426.6(WT1):c.498T>C (p.Thr166=) rs1554946487
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682
NM_024426.6(WT1):c.555C>T (p.Phe185=) rs1554946465
NM_024426.6(WT1):c.585C>T (p.Ser195=) rs1332888095
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583
NM_024426.6(WT1):c.633C>T (p.Leu211=) rs576677344
NM_024426.6(WT1):c.75C>T (p.Ser25=) rs1417997475
NM_024426.6(WT1):c.87C>T (p.Cys29=) rs1554946770

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.