ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.4331A>G (p.Asn1444Ser)

gnomAD frequency: 0.00003  dbSNP: rs567013299
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000861512 SCV001001850 benign Primary ciliary dyskinesia 2023-11-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717716 SCV005306057 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV000861512 SCV001467487 likely benign Primary ciliary dyskinesia 2020-09-16 no assertion criteria provided 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.