ClinVar Miner

Submissions for variant NM_001002294.3(FMO3):c.1079T>C (p.Leu360Pro)

gnomAD frequency: 0.00158  dbSNP: rs28363581
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
Invitae RCV002513145 SCV003289499 likely benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneReviews RCV000020652 SCV000041185 not provided Trimethylaminuria no assertion 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.