ClinVar Miner

List of variants in gene OPA3 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025136.4(OPA3):c.231T>C (p.Ala77=) rs3826860 0.70508
NM_025136.4(OPA3):c.*1950G>A rs4404183 0.69999
NM_025136.4(OPA3):c.*152G>A rs3826861 0.66011
NM_025136.4(OPA3):c.*6012A>G rs11083772 0.57481
NM_001017989.3(OPA3):c.143-16698C>A rs11672063 0.43859
NM_001017989.3(OPA3):c.143-127C>G rs12971437 0.37215
NM_025136.4(OPA3):c.*638T>A rs150575877 0.13416
NM_001017989.3(OPA3):c.143-23_143-22del rs149252540 0.12886
NM_025136.4(OPA3):c.*3212G>A rs79317386 0.11204
NM_001017989.3(OPA3):c.*190A>G rs73568948 0.08035
NM_025136.4(OPA3):c.*577T>C rs112654759 0.06094
NC_000019.10:g.45585093A>T rs58173251 0.05614
NM_025136.4(OPA3):c.*272G>A rs7246349 0.05540
NM_025136.4(OPA3):c.*3038G>A rs73568982 0.05112
NM_001017989.3(OPA3):c.143-16757T>C rs115090385 0.01529
NM_025136.4(OPA3):c.412G>A (p.Ala138Thr) rs201574732 0.00477
NM_025136.4(OPA3):c.*3111AGC[3] rs542311224
NM_025136.4(OPA3):c.*4850_*4852del rs144752998
NM_025136.4(OPA3):c.*4857A>T rs4803833
NM_025136.4(OPA3):c.*5809dup rs58766088

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.