rs2272783(C;T)
From SNPedia
| Low expression variant of FECH enzyme |
| Is a | genotype |
| of | rs2272783 |
| Gene | FECH |
| Chromosome | 18 |
| Position | 57,571,588 |
| mentioned | by |
| Magnitude | 2.2 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 4 | likely erythropoietic protoporphyria symptoms |
| (C;T) | 2.2 | Low expression variant of FECH enzyme |
| (T;T) | 0 | common in clinvar |
If your other FECH allele is normal, you are most likely asymptomatic. However, if you harbor this rs2272783(C;T) genotype AND your other FECH allele is actually nonfunctional, you are likely to have symptoms associated with Erythropoietic protoporphyria.
