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rs33986703(A;A)

From SNPedia

common in complete genomics
Is agenotype
ofrs33986703
GeneHBB
Chromosome11
Position5,226,970
Merged fromRs74576531
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in complete genomics
(A;T) 3 Beta Thalassemia carrier; Hemoglobin beta-zero mutation; anemia possible
(AA;AA) 0 common in clinvar
(T;T) 5.5 Beta Thalassemia major; Hemoglobin beta-zero; possibly transfusion dependent