ClinVar Miner

Submissions for variant NM_003619.4(PRSS12):c.2128dup (p.Gln710fs)

gnomAD frequency: 0.00002  dbSNP: rs757141803
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
Genetic Services Laboratory, University of Chicago RCV000499463 SCV000596605 uncertain significance not specified 2016-12-27 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002481624 SCV002783046 uncertain significance Intellectual disability, autosomal recessive 1 2021-11-12 criteria provided, single submitter 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.