ClinVar Miner

Submissions for variant NM_020879.3(CCDC146):c.1084C>T (p.Arg362Ter)

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
Genetics of Infertility and Preimplantation Genetic Diagnosis, Centre Hospitalier Universitaire Grenoble Alpes RCV003881709 SCV004697441 pathogenic Male infertility due to sperm motility disorder 2024-02-07 no assertion criteria provided clinical testing
OMIM RCV004577046 SCV005060856 pathogenic Spermatogenic failure 94 2024-06-11 no assertion criteria provided literature only

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.