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rs33913413(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs33913413
GeneHBB
Chromosome11
Position5,225,729
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 3 Beta Thalassemia carrier; Hemoglobin beta-plus mutation
(G;G) 4.5 Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms