ClinVar Miner

Submissions for variant NM_000532.5(PCCB):c.372+31T>C

gnomAD frequency: 0.00526  dbSNP: rs16843829
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
PreventionGenetics, part of Exact Sciences RCV000242229 SCV000304709 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001651133 SCV001863884 benign not provided 2018-07-27 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.