rs34598529(G;G)
From SNPedia
| Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms |
| Is a | genotype |
| of | rs34598529 |
| Gene | HBB |
| Chromosome | 11 |
| Position | 5,227,100 |
| mentioned | by |
| Magnitude | 4.5 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| (A;G) | 3 | Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
| (G;G) | 4.5 | Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms |
see HBB Beta thalassemia is a genetic blood disorder that can cause anemia.
the most common mutation in people with African ancestry.
