ClinVar Miner

Submissions for variant NM_002739.5(PRKCG):c.534C>T (p.Gly178=)

gnomAD frequency: 0.00002  dbSNP: rs367543207
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 RCV000084800 SCV001057455 likely benign not provided 2018-12-10 criteria provided, single submitter clinical testing
Psychiatry Genetics Yale University RCV000084800 SCV000116936 not provided not provided no assertion provided not provided

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.