rs1427407, BCL11A

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sickle Cell Trait
CUI: C0037054
Disease: Sickle Cell Trait
0.010 GeneticVariation BEFREE The current study was conducted on 240 patients with SCD and 60 with sickle cell trait, to determine the association of genetic variants at the BCL11A (rs1427407) and HBS1-MYB (rs6934903) loci with fetal hemoglobin levels (HbF). 25457385 2015