ClinVar Miner

Submissions for variant NM_001329.4(CTBP2):c.1218C>A (p.Ile406=)

dbSNP: rs796230948
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
CeGaT Center for Human Genetics Tuebingen RCV001357724 SCV004134839 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing CTBP2: PM2:Supporting, BP4, BP7
Department of Pathology and Laboratory Medicine, Sinai Health System RCV001357724 SCV001553277 uncertain significance not provided no assertion criteria provided 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.