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rs33981098(A;A)

From SNPedia

common in complete genomics
Is agenotype
ofrs33981098
GeneHBB
Chromosome11
Position5,227,102
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in complete genomics
(A;C) 3 Beta Thalassemia carrier; Hemoglobin beta-plus mutation
(C;C) 4.5 Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms