rs33978907(T;T)
From SNPedia
common in complete genomics |
Is a | genotype |
of | rs33978907 |
Gene | HBB |
Chromosome | 11 |
Position | 5,225,488 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(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 complete genomics |
(TA;TA) | 0 | common in clinvar |