Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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: 1457
Gene Symbol: CSNK2A1
CSNK2A1 		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: 8131
Gene Symbol: NPRL3
NPRL3 		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: 53335
Gene Symbol: BCL11A
BCL11A 		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: 3046
Gene Symbol: HBE1
HBE1 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L 		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: 4676
Gene Symbol: NAP1L4
NAP1L4 		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: 3046
Gene Symbol: HBE1
HBE1 		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: 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: 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: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype GWASCAT 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: 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: 101927763
Gene Symbol: OLFM5P
OLFM5P 		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: 3045
Gene Symbol: HBD
HBD 		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: 3043
Gene Symbol: HBB
HBB 		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: 3048
Gene Symbol: HBG2
HBG2 		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: 3046
Gene Symbol: HBE1
HBE1 		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: 282763
Gene Symbol: OR51B5
OR51B5 		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: 3048
Gene Symbol: HBG2
HBG2 		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