ClinVar Miner

List of variants in gene DNM2 reported as benign by PreventionGenetics,PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
NM_001005360.2(DNM2):c.1077C>T (p.Gly359=) rs112238216
NM_001005360.2(DNM2):c.1129-40C>T rs199742926
NM_001005360.2(DNM2):c.1545+14C>G rs114713494
NM_001005360.2(DNM2):c.1545+41C>T rs2287029
NM_001005360.2(DNM2):c.2139T>C (p.Ala713=) rs2229920
NM_001005360.2(DNM2):c.2160C>T (p.Asp720=) rs117598326
NM_001005360.2(DNM2):c.235+12C>A rs147026993
NM_001005360.2(DNM2):c.235+6A>G rs113192269
NM_001005360.2(DNM2):c.236-29C>G rs3826803
NM_001005360.2(DNM2):c.2484G>A (p.Pro828=) rs114682382

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.