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rs281864900(CTTT;CTTT)

From SNPedia

common in clinvar
Is agenotype
ofrs281864900
GeneHBB
Chromosome11
Position5,226,763
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;-) Usually transfusion-dependent.
(-;CTTT) Typical for a beta zero-thal heterozygote with modest anemia, microcytosis, and hypochromia
(CTTT;CTTT) 0 common in clinvar