ClinVar Miner

List of variants in gene combination DPM2, LOC130002675 reported as uncertain significance for disorder of multiple glycosylation

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_003863.3(DPM2):c.-211T>G rs187834148 0.00027
NM_003863.3(DPM2):c.-141G>A rs886063485 0.00016
NM_003863.4(DPM2):c.-5G>A rs371551833 0.00008
NM_003863.4(DPM2):c.3+6A>G rs776375979 0.00002
NM_003863.3(DPM2):c.-208G>A rs1290789503 0.00001
NM_003863.3(DPM2):c.-88C>T rs886063484 0.00001
NM_003863.4(DPM2):c.3+5G>A rs1333396682 0.00001
NM_003863.3(DPM2):c.-267T>C rs1831540551
NM_003863.3(DPM2):c.-84G>A rs1831537719
NM_003863.4(DPM2):c.3+3G>A rs1403906360
NM_003863.4(DPM2):c.3+3G>T rs1403906360

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.