ClinVar Miner

List of variants in gene NEXN reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP
NM_001172309.1(NEXN):c.*4_*5CT[1] rs553696163
NM_001172309.1(NEXN):c.-212_-210GGC[7] rs528439602
NM_144573.3(NEXN):c.*418del rs368295679
NM_144573.3(NEXN):c.1228C>T (p.Gln410Ter) rs1557988499
NM_144573.3(NEXN):c.1606_1607del (p.Lys536fs) rs1394704286
NM_144573.3(NEXN):c.1892T>C (p.Ile631Thr) rs775292649

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.