ClinVar Miner

Submissions for variant NM_012472.6(DNAAF11):c.914+13A>G

gnomAD frequency: 0.00652  dbSNP: rs113135637
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
PreventionGenetics, part of Exact Sciences RCV000244928 SCV000311957 benign not specified criteria provided, single submitter clinical testing
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514254 SCV000610236 likely benign not provided 2017-08-28 criteria provided, single submitter clinical testing
Invitae RCV002230202 SCV002508817 benign Primary ciliary dyskinesia 19 2024-01-25 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.