rs1049296(C;T)
From SNPedia
| Heterozygote carrying both C1 and C2 transferrin subtypes; very slightly higher risk for Alzheimers |
| Is a | genotype |
| of | rs1049296 |
| Gene | TF |
| Chromosome | 3 |
| Position | 133,775,510 |
| mentioned | by |
| Magnitude | 1.1 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | C1 subtype of transferrin; common in clinvar |
| (C;T) | 1.1 | Heterozygote carrying both C1 and C2 transferrin subtypes; very slightly higher risk for Alzheimers |
| (T;T) | 1.2 | C2 transferrin subtype; very slightly higher risk for Alzheimers |
