ClinVar Miner

Submissions for variant NM_020812.4(DOCK6):c.906G>C (p.Ser302=)

dbSNP: rs79202547
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
CeGaT Center for Human Genetics Tuebingen RCV000512706 SCV000608875 likely benign not provided 2024-07-01 criteria provided, single submitter clinical testing DOCK6: BP4, BP7
Invitae RCV000512706 SCV001102263 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003900064 SCV004711267 likely benign DOCK6-related disorder 2021-02-10 criteria provided, single submitter clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.