rs1736557(A;A)
From SNPedia
| normal? |
| Is a | genotype |
| of | rs1736557 |
| Gene | FMO3 |
| Chromosome | 1 |
| Position | 171,110,939 |
| Merged from | Rs17858963 |
| mentioned | by |
| Magnitude | 1.1 |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 1.1 | normal? |
| (A;G) | 0 | unlikely to be associated with trimethylaminuria unless as a carrier (if that) |
| (G;G) | 0 | common in clinvar |
This missense homozgous genotype has been reported to be associated with trimethylaminuria, yet other reports indicate it may be a benign polymorphism. One SNPedia self reports this genotype, with no symptoms. Feel free to share your findings/beliefs with SNPedia if you have this genotype.
