ClinVar Miner

Submissions for variant NM_001127255.2(NLRP7):c.2811-25G>C

gnomAD frequency: 0.06249  dbSNP: rs775870
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV001293268 SCV001481860 benign Hydatidiform mole 2021-02-22 criteria provided, single submitter research
Breakthrough Genomics, Breakthrough Genomics RCV004716939 SCV005312807 benign not provided criteria provided, single submitter not provided
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000084023 SCV000116146 not provided Hydatidiform mole, recurrent, 1 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.