ClinVar Miner

Submissions for variant NM_003356.4(UCP3):c.127-7C>T

gnomAD frequency: 0.00848  dbSNP: rs77012485
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000897300 SCV001041439 benign not provided 2023-12-11 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818726 SCV002066327 benign not specified 2018-09-27 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002479029 SCV002798003 likely benign Obesity 2021-10-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000897300 SCV005235213 benign not provided criteria provided, single submitter 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.