ClinVar Miner

Submissions for variant NM_019066.5(MAGEL2):c.1404CCCACCTGTGATCCGCCAGGC[1] (p.464VIRQAPP[3])

dbSNP: rs1386125417
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000593663 SCV000704593 uncertain significance not provided 2017-01-16 criteria provided, single submitter clinical testing
Invitae RCV000593663 SCV001110257 benign not provided 2024-01-30 criteria provided, single submitter clinical testing
GeneDx RCV000593663 SCV001985089 benign not provided 2021-08-12 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000593663 SCV004129375 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing MAGEL2: BS2

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.