ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.893-92C>T

gnomAD frequency: 0.03881  dbSNP: rs72803305
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 RCV001672011 SCV001888166 benign not provided 2018-09-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002253944 SCV002524210 benign KBG syndrome 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001672011 SCV005253186 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.