ClinVar Miner

Submissions for variant NM_001348323.3(TRIP12):c.3482+15G>A

gnomAD frequency: 0.36718  dbSNP: rs6720868
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
GeneDx RCV001608625 SCV001835468 benign not provided 2019-05-02 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838692 SCV002098787 benign Clark-Baraitser syndrome 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001608625 SCV005243477 benign not provided criteria provided, single submitter 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.