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rs35662066(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs35662066
GeneHBB
Chromosome11
Position5,226,971
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 5.5 Beta Thalassemia major; Hemoglobin beta-zero; possibly transfusion dependent
(-;C) 3 Beta Thalassemia carrier; Hemoglobin beta-zero mutation; anemia possible
(C;C) 0 common in clinvar