ClinVar Miner

Submissions for variant NM_000789.3(ACE):c.2306-117_2306-116insAF118569.1:g.14094_14382

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 7
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000019678 SCV000039976 benign ANGIOTENSIN I-CONVERTING ENZYME INSERTION/DELETION POLYMORPHISM 2009-02-17 no assertion criteria provided literature only
OMIM RCV000019679 SCV000039977 risk factor Myocardial infarction 2009-02-17 no assertion criteria provided literature only
OMIM RCV000019680 SCV000039978 risk factor Microvascular complications of diabetes 3 2009-02-17 no assertion criteria provided literature only
OMIM RCV000019681 SCV000039979 risk factor Stroke, hemorrhagic, susceptibility to 2009-02-17 no assertion criteria provided literature only
OMIM RCV000019682 SCV000039980 risk factor Ischemic stroke, susceptibility to 2009-02-17 no assertion criteria provided literature only
OMIM RCV000019683 SCV000039981 pathogenic Severe acute respiratory syndrome, progression of 2009-02-17 no assertion criteria provided literature only
OMIM RCV000019684 SCV000039982 risk factor Susceptibility to progression to renal failure in IgA nephropathy 2009-02-17 no assertion criteria provided literature only

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.