ClinVar Miner

Submissions for variant NM_152564.5(VPS13B):c.1612A>G (p.Met538Val)

gnomAD frequency: 0.00001  dbSNP: rs1478296228
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001245051 SCV001418313 uncertain significance Cohen syndrome 2021-08-27 criteria provided, single submitter clinical testing
Natera, Inc. RCV001245051 SCV002079476 uncertain significance Cohen syndrome 2019-10-29 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.