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Figure 2 | BMC Genomics

Figure 2

From: Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach

Figure 2

Sequence variations close to SNP rs7775698. Nucleotide sequences between chromosome 6: 135460308 to 135460368 bp. The sequences shown are: the rs7775698 major allele C, the rs7775698 minor allele T, the rs371998411 (CTA) 3 bp deletion, the rs66650371 (TAC) 3 bp deletion and the rs55634702 (TA) 2 bp insertion. In red is indicated the sequence variation.

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