rs33981098(A;C)
From SNPedia
| Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
| Is a | genotype |
| of | rs33981098 |
| Gene | HBB |
| Chromosome | 11 |
| Position | 5,227,102 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| (A;C) | 3 | Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
| (C;C) | 4.5 | Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms |
Unaffected in absence of a second HBB gene mutation; see discussion at HBB
