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rs34690599(G;G)

From SNPedia

Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms
Is agenotype
ofrs34690599
GeneHBB
Chromosome11
Position5,225,832
mentionedby
Magnitude4.5
ReputeBad
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

see HBB