ClinVar Miner

List of variants in gene GNE reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_001128227.3(GNE):c.51+17T>G rs144416128
NM_005476.7(GNE):c.1233C>T (p.Ala411=) rs1057523203
NM_005476.7(GNE):c.1245C>A (p.Gly415=) rs140784655
NM_005476.7(GNE):c.1245C>T (p.Gly415=) rs140784655
NM_005476.7(GNE):c.1281+44G>A rs16933102
NM_005476.7(GNE):c.1281+6A>T rs201025841
NM_005476.7(GNE):c.1293T>A (p.Val431=) rs143485388
NM_005476.7(GNE):c.165-18A>G rs374105190
NM_005476.7(GNE):c.165-9C>T rs760509369
NM_005476.7(GNE):c.1872G>A (p.Ala624=) rs145361930
NM_005476.7(GNE):c.1908G>A (p.Ala636=) rs200812140
NM_005476.7(GNE):c.1934-36T>A rs375573973
NM_005476.7(GNE):c.624T>G (p.Asp208Glu) rs35224402
NM_005476.7(GNE):c.765C>T (p.Asp255=) rs775805166
NM_005476.7(GNE):c.804G>A (p.Lys268=) rs141814943
NM_005476.7(GNE):c.843C>T (p.His281=) rs138694766

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.