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rs11549407(CA;CA)

From SNPedia

common in clinvar
Is agenotype
ofrs11549407
GeneHBB
Chromosome11
Position5,226,774
Merged fromRs76728603
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in complete genomics
(C;T) 3 Beta Thalassemia carrier; Hemoglobin beta-zero mutation; anemia possible
(CA;CA) 0 common in clinvar
(T;T) 5.5 Beta Thalassemia major; Hemoglobin beta-zero