ClinVar Miner

List of variants in gene WRN reported by Mendelics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP
NM_000553.6(WRN):c.1351-1G>A rs1170732591
NM_000553.6(WRN):c.3437C>T (p.Ser1146Leu) rs779264260
NM_000553.6(WRN):c.3785C>G (p.Thr1262Arg) rs78488552
NM_000553.6(WRN):c.3881C>T (p.Ala1294Val) rs146861737
NM_000553.6(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
NM_000553.6(WRN):c.4216C>T (p.Arg1406Ter) rs11574410
NM_000553.6(WRN):c.839+25del rs370040831

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.