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rs33978907(T;T)

From SNPedia

common in complete genomics
Is agenotype
ofrs33978907
GeneHBB
Chromosome11
Position5,225,488
mentionedby
Magnitude0
ReputeGood
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