ClinVar Miner

Submissions for variant NM_033641.4(COL4A6):c.3809-14G>A

gnomAD frequency: 0.00032  dbSNP: rs192754010
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 RCV001643352 SCV001857900 benign not provided 2020-01-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001643352 SCV002365494 benign not provided 2025-01-22 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002271279 SCV002555087 benign Hearing loss, X-linked 6 2022-03-15 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.