rs34690599(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs34690599 |
| Gene | HBB |
| Chromosome | 11 |
| Position | 5,225,832 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;G) | 3 | Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
| (G;G) | 4.5 | Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms |
