ClinVar Miner

List of variants in gene WRN reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
NM_000553.6(WRN):c.1161G>A (p.Met387Ile) rs1800391
NM_000553.6(WRN):c.1577-3C>A rs3087409
NM_000553.6(WRN):c.2361G>T (p.Leu787=) rs1800392
NM_000553.6(WRN):c.3138+6C>T rs3024239
NM_000553.6(WRN):c.3222G>T (p.Leu1074Phe) rs1801195
NM_000553.6(WRN):c.3236C>T (p.Ser1079Leu) rs3087414
NM_000553.6(WRN):c.4083C>T (p.Ser1361=) rs1801196
NM_000553.6(WRN):c.4099T>C (p.Cys1367Arg) rs1346044
NM_000553.6(WRN):c.513C>T (p.Cys171=) rs1800389

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.