rs10195871, BCL11A

N. diseases: 2
Disease: Fetal hemoglobin determination ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
0.800 GeneticVariation GWASDB Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. 22936743 2012
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
0.800 GeneticVariation GWASCAT Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
0.800 GeneticVariation GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
0.800 GeneticVariation GWASDB A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. 17767159 2007