ClinVar Miner

Submissions for variant NM_000025.3(ADRB3):c.190T>C (p.Trp64Arg)

gnomAD frequency: 0.09116  dbSNP: rs4994
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
GeneDx RCV001707510 SCV001935767 benign not provided 2021-06-09 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 9080262, 29670643, 22774474, 11380082, 21529759, 23729572, 21289629, 21358132, 20008926, 20069060, 11564599, 17225053, 19553224, 22550477, 19133996, 21285172, 21034552, 19080138, 7487991, 28456594, 23968135, 20078877, 23032405)
Breakthrough Genomics, Breakthrough Genomics RCV001707510 SCV005264832 benign not provided criteria provided, single submitter not provided
OMIM RCV000033197 SCV000057043 risk factor Obesity 2004-10-01 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.