ClinVar Miner

List of variants reported as benign for Trimethylaminuria

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001002294.3(FMO3):c.485-22G>A rs1920149 0.53900
NM_001002294.3(FMO3):c.472G>A (p.Glu158Lys) rs2266782 0.40810
NM_001002294.3(FMO3):c.855C>T (p.Asn285=) rs909530 0.31712
NM_001002294.3(FMO3):c.627+10C>G rs2066534 0.21613
NM_001002294.3(FMO3):c.923A>G (p.Glu308Gly) rs2266780 0.13897
NM_001002294.3(FMO3):c.441C>T (p.Ser147=) rs1800822 0.07828
NM_001002294.3(FMO3):c.769G>A (p.Val257Met) rs1736557 0.06174
NM_001002294.3(FMO3):c.394G>C (p.Asp132His) rs12072582 0.01253
NM_001002294.3(FMO3):c.539G>T (p.Gly180Val) rs75904274 0.01197
NM_001002294.3(FMO3):c.1221T>C (p.Asn407=) rs79553697 0.00376

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.