Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 143630
Gene Symbol: UBQLNL
UBQLNL 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 85363
Gene Symbol: TRIM5
TRIM5 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 143425
Gene Symbol: SYT9
SYT9 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 6786
Gene Symbol: STIM1
STIM1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 6240
Gene Symbol: RRM1
RRM1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 63935
Gene Symbol: PCIF1
PCIF1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 283110
Gene Symbol: OR52Z1
OR52Z1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 81246
Gene Symbol: OR52Q1P
OR52Q1P 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 79529
Gene Symbol: OR52J2P
OR52J2P 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 143502
Gene Symbol: OR52I2
OR52I2 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 81261
Gene Symbol: OR52H2P
OR52H2P 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 390082
Gene Symbol: OR52E5
OR52E5 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 81270
Gene Symbol: OR52B5P
OR52B5P 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 79300
Gene Symbol: OR51P1P
OR51P1P 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 119696
Gene Symbol: OR51N1P
OR51N1P 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 390059
Gene Symbol: OR51M1
OR51M1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 119682
Gene Symbol: OR51L1
OR51L1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 390063
Gene Symbol: OR51I1
OR51I1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 81282
Gene Symbol: OR51G2
OR51G2 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 256892
Gene Symbol: OR51F1
OR51F1 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 81285
Gene Symbol: OR51E2
OR51E2 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 390058
Gene Symbol: OR51B6
OR51B6 		0.100 GeneticVariation phenotype GWASDB Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. 22936743 2012
Entrez Id: 390058
Gene Symbol: OR51B6
OR51B6 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Entrez Id: 390058
Gene Symbol: OR51B6
OR51B6 		0.100 GeneticVariation phenotype GWASCAT Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. 20018918 2010
Entrez Id: 390058
Gene Symbol: OR51B6
OR51B6 		0.100 GeneticVariation phenotype GWASDB Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. 20018918 2010