ClinVar Miner

Submissions for variant NM_012203.1(GRHPR):c.866-25CT[9]

dbSNP: rs34302950
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 5
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241767 SCV000311879 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001709515 SCV001938801 benign not provided 2020-06-02 criteria provided, single submitter clinical testing
Invitae RCV001709515 SCV002446359 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneReviews RCV000186434 SCV000041225 benign Primary hyperoxaluria, type II 2011-05-05 no assertion criteria provided curation Converted during submission to Benign.
Clinical Biochemistry Laboratory, Health Services Laboratory RCV000186434 SCV000239786 uncertain significance Primary hyperoxaluria, type II 2014-11-27 no assertion criteria provided research

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.