ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.896+6669TC[12]

dbSNP: rs71019410
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000036851 SCV000060506 likely benign not specified 2011-10-12 criteria provided, single submitter clinical testing 756-15_756-12delCTCT in intron 7 of LDB3: This variant is not expected to have c linical significance because it is not located in the conserved +/- 1, 2 region of the splicing consensus sequence.
Eurofins Ntd Llc (ga) RCV000036851 SCV000332565 benign not specified 2015-07-14 criteria provided, single submitter clinical testing
GeneDx RCV001668154 SCV001883480 benign not provided 2019-08-13 criteria provided, single submitter clinical testing

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.