Figure 2From: Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approachSequence variations close to SNP rs7775698. Nucleotide sequences between chromosome 6: 135460308 to 135460368Â bp. The sequences shown are: the rs7775698 major allele C, the rs7775698 minor allele T, the rs371998411 (CTA) 3Â bp deletion, the rs66650371 (TAC) 3Â bp deletion and the rs55634702 (TA) 2Â bp insertion. In red is indicated the sequence variation.Back to article page