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rs63751128(A;A)

From SNPedia

common in clinvar
Is agenotype
ofrs63751128
GeneHBB
Chromosome11
Position5,225,487
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Beta Thalassemia carrier; Hemoglobin beta-plus mutation
(G;G) 4.5 Beta Thalassemia intermedia likely; Hemoglobin beta-plus; variable clinical symptoms