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rs63749819(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs63749819
GeneHBB
Chromosome11
Position5,227,002
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) 5.5 Beta Thalassemia major; Hemoglobin beta-zero; possibly transfusion dependent
(-;A) 3 Beta Thalassemia carrier; Hemoglobin beta-zero mutation; anemia possible
(A;A) 0 common in clinvar