ClinVar Miner

Submissions for variant NM_015294.6(TRIM37):c.810-13dup

dbSNP: rs367700401
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
Illumina Laboratory Services, Illumina RCV000296131 SCV000404363 uncertain significance Mulibrey nanism syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000676024 SCV001764903 likely benign not provided 2019-08-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000676024 SCV002408809 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV000676024 SCV000801758 likely benign not provided 2018-03-01 no assertion criteria provided 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.