ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.5816G>A (p.Arg1939Gln)

gnomAD frequency: 0.00001  dbSNP: rs1024797402
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
Athena Diagnostics RCV000991797 SCV001143551 uncertain significance not provided 2018-09-18 criteria provided, single submitter clinical testing
GeneDx RCV000991797 SCV001992431 uncertain significance not provided 2019-04-23 criteria provided, single submitter clinical testing In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV005056721 SCV005716862 benign CHARGE syndrome 2024-02-19 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.