ClinVar Miner

List of variants in gene NEXN reported as uncertain significance by Stanford Center for Inherited Cardiovascular Disease,Stanford University

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_144573.3(NEXN):c.1416_1418AAG[1] (p.Arg475del) rs794729091
NM_144573.3(NEXN):c.1435C>T (p.Leu479Phe) rs181520023
NM_144573.3(NEXN):c.1671_1673GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.3(NEXN):c.1918_1922del (p.Tyr640fs) rs1222794437
NM_144573.3(NEXN):c.1935C>G (p.Phe645Leu) rs794729086
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.