ClinVar Miner

List of variants in gene NEXN reported as likely benign by CHEO Genetics Diagnostic Laboratory,Children's Hospital of Eastern Ontario

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_144573.3(NEXN):c.1065T>C (p.Asp355=) rs369897647
NM_144573.3(NEXN):c.1605A>G (p.Gln535=) rs778477679
NM_144573.3(NEXN):c.216G>A (p.Gln72=) rs531315786
NM_144573.3(NEXN):c.249G>A (p.Glu83=) rs372532824
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096

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.