ClinVar Miner

List of variants in gene WRN reported as pathogenic by OMIM

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_000553.4(WRN):c.3690_3693delAGAC (p.Asp1231Serfs) rs606231162
NM_000553.6(WRN):c.1105C>T (p.Arg369Ter) rs17847577
NM_000553.6(WRN):c.1730A>T (p.Lys577Met) rs121908448
NM_000553.6(WRN):c.3139-1G>C rs113993961
NM_000553.6(WRN):c.3493C>T (p.Gln1165Ter) rs121908447
NM_000553.6(WRN):c.3686A>T (p.Gln1229Leu) rs369158322
NM_000553.6(WRN):c.3913C>T (p.Arg1305Ter) rs121908446
NM_000553.6(WRN):c.3915dup (p.Ala1306fs) rs587776621
RECQL2, 1-BP DEL, NT1396

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.