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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation
Geneviève Galarneau1, Cameron D Palmer, Vijay G Sankaran
1Montreal Heart Institute, Montréal, Québec, Canada.
None:
We used resequencing and genotyping in African Americans with sickle cell anemia (SCA) to characterize associations with fetal hemoglobin (HbF) levels at the BCL11A, HBS1L-MYB and β-globin loci. Fine-mapping of HbF association signals at these loci confirmed seven SNPs with independent effects and increased the explained heritable variation in HbF levels from 38.6% to 49.5%. We also identified rare missense variants that causally implicate MYB in HbF production.
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