ClinVar Miner

Submissions for variant NM_024312.5(GNPTAB):c.1863C>T (p.Asn621=)

dbSNP: rs758930596
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 RCV000975378 SCV001123261 likely benign Mucolipidosis type II; Pseudo-Hurler polydystrophy 2023-11-17 criteria provided, single submitter clinical testing
Natera, Inc. RCV001827066 SCV002088584 likely benign Mucolipidosis type II 2021-10-12 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.