ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.4197C>T (p.Ile1399=)

gnomAD frequency: 0.00306  dbSNP: rs35583018
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000887610 SCV001031180 benign not provided 2025-01-30 criteria provided, single submitter clinical testing
GeneDx RCV000887610 SCV001782750 likely benign not provided 2019-08-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000887610 SCV004137827 benign not provided 2023-03-01 criteria provided, single submitter clinical testing DOCK6: BP4, BP7, BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000887610 SCV005209425 likely 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.