Later studies showed that these three SNPs were associated with HbF levels in sickle cell disease (SCD) patients from other populations: African American and Brazilian [6], African British [7] and [11], and Tanzanian [7]. HMIP-2 is characterized by eleven LGK-974 solubility dmso SNPs, all of which have shown a strong association with HbF levels in Europe, but only some of them have shown a significant association in SCD African ancestry patients [9] and [11]. The MAF of rs9399137 (C), considered the most significantly associated with HbF expression, is less common in African populations, with frequencies of 1–2% in African descendant SCA patients without European

admixture [7] and [11]. Similarly, a 3-bp (TAC) deletion, which is in complete LD with the minor allele of rs9399137 and considered as the functional motif for this QTL, is also more common in non-African populations [12]. However, the minor allele of rs9399137 (C) was

found with significantly higher frequencies in African American SCA patients with HbF unusually selleck chemicals higher than among patients with low HbF (18% versus 3%; P = 0.02) [8]. The authors suggested that some patients with markedly elevated HbF might have inherited the minor allele of rs9399137 due to European genetic admixture. In summary, the HBS1L-MYB intergenic polymorphism is also associated with HbF among SCA patients of African ancestry, although much less significantly so when compared with European and Chinese patients because of their much lower MAF (review

in [4]). Positive association between the MAF of rs7482144 (A), in the Gγ-globin (HBG2) gene promoter, and HbF levels, has been well documented in Tanzanian patients selected from the Muhimbili Sickle Cell Collaborative Program [6], in Dar-es-Salaam [7], and in African American SCD patients selected from the Cooperative Study of Sickle Cell Disease (CSSCD) [13]. However, no significant effects of rs7482144 on HbF levels were found in African British patients cAMP of African-Caribbean (Jamaican, Trinidanian) or West African (Nigerian, Ghanaian, Sierra Leonean) descent, selected from King’s College Hospital, in London, nor in African Brazilian patients from the State of Pernambuco, Brazil — northeastern region [6]. Further evidence of the influence of rs7482144 on HbF levels has been obtained in African–American patients also selected from the CSSCD when patients with high levels of HbF who showed the minor allele (A) presented a frequency significantly higher than that found among those with low levels of HbF (30% versus 10%, P = 0.002). However, the frequencies of the A allele of rs7482144 were not different between high and low HbF groups in another sample of African–American SCA patients selected from the Reference Laboratory Diagnosis of hemoglobin in the Boston Medical Center (10% versus 8%, respectively, P = 1.0) [8].