ClinVar Miner

Submissions for variant NM_000350.3(ABCA4):c.1761-37G>A

gnomAD frequency: 0.00491  dbSNP: rs61754021
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000085421 SCV001840581 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Retina International RCV000085421 SCV000117558 not provided not provided no assertion provided not provided

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.