rs35724775(C;C)
From SNPedia
Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms |
Is a | genotype |
of | rs35724775 |
Gene | HBB |
Chromosome | 11 |
Position | 5,226,924 |
mentioned | by |
Magnitude | 4.5 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | |
(C;C) | 4.5 | Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms |
(C;T) | 3 | Beta Thalassemia carrier; Hemoglobin beta-plus mutation |
(T;T) | 0 | common in clinvar |
see HBB