ClinVar Miner

List of variants in gene combination LOC107982234, WT1 reported as benign for Wilms tumor type 1

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
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.309C>A (p.Gly103=) rs547333427
NM_024426.6(WT1):c.345C>T (p.Pro115=) rs1799925
NM_024426.6(WT1):c.375C>T (p.Gly125=) rs776209354
NM_024426.6(WT1):c.513C>A (p.Gly171=) rs536728682
NM_024426.6(WT1):c.543C>T (p.Arg181=) rs369870529
NM_024426.6(WT1):c.609C>T (p.Asn203=) rs2234583

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.