ClinVar Miner

List of variants in gene LEP reported as likely benign for congenital hypogonadotropic hypogonadism

Included ClinVar conditions (68):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000230.3(LEP):c.*2205G>A rs41457646 0.10795
NM_000230.3(LEP):c.*400G>T rs17151922 0.09344
NM_000230.3(LEP):c.*1243A>G rs6966536 0.02955
NM_000230.3(LEP):c.280G>A (p.Val94Met) rs17151919 0.02565
NM_000230.3(LEP):c.*2595C>A rs28959475
NM_000230.3(LEP):c.*2820_*2822dup rs56247456

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.