ClinVar Miner

List of variants in gene LMNB2 reported as benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP
NM_032737.4(LMNB2):c.1247G>T (p.Arg416Leu) rs200293412
NM_032737.4(LMNB2):c.1554G>C (p.Thr518=) rs11882908
NM_032737.4(LMNB2):c.255C>G (p.Thr85=) rs201524951
NM_032737.4(LMNB2):c.704G>A (p.Arg235Gln) rs121912497
NM_032737.4(LMNB2):c.804C>T (p.Asp268=) rs150969746

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.