ClinVar Miner

List of variants in gene UMOD reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_003361.3(UMOD):c.*226_*229del rs886051782
NM_003361.3(UMOD):c.*231A>G rs886051781
NM_003361.3(UMOD):c.*59G>A rs886051783
NM_003361.3(UMOD):c.1131G>C (p.Trp377Cys) rs201738891
NM_003361.3(UMOD):c.1177T>C (p.Leu393=) rs748849021
NM_003361.3(UMOD):c.1182+5G>T rs755374625
NM_003361.3(UMOD):c.1406C>T (p.Thr469Met) rs143583842
NM_003361.3(UMOD):c.1680C>G (p.Asp560Glu) rs200473249
NM_003361.3(UMOD):c.1859dup (p.Leu620fs) rs886051784
NM_003361.3(UMOD):c.865+7C>G rs759063012

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.