ClinVar Miner

Submissions for variant NM_016032.4(ZDHHC9):c.291G>A (p.Ala97=)

gnomAD frequency: 0.00035  dbSNP: rs77513704
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000914795 SCV001059980 benign Syndromic X-linked intellectual disability Raymond type 2024-01-26 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003438585 SCV004165551 likely benign not provided 2022-09-01 criteria provided, single submitter clinical testing ZDHHC9: BP4, BP7

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.