ClinVar Miner

Submissions for variant NM_000521.4(HEXB):c.160C>A (p.Pro54Thr)

dbSNP: rs778119481
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000691227 SCV000818976 likely benign Sandhoff disease 2023-11-24 criteria provided, single submitter clinical testing
Daryl Scott Lab, Baylor College of Medicine RCV000691227 SCV004102695 pathogenic Sandhoff disease 2023-11-10 criteria provided, single submitter clinical testing
Natera, Inc. RCV000691227 SCV002084932 uncertain significance Sandhoff disease 2019-10-28 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.