rs63751208(C;T)
From SNPedia
| Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
| Is a | genotype |
| of | rs63751208 |
| Gene | HBB |
| Chromosome | 11 |
| Position | 5,227,172 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
| (T;T) | 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
