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: 3050
Gene Symbol: HBZ
HBZ 		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 analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels. 26366553 2015
Entrez Id: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype GWASCAT Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. 27022141 2016
Entrez Id: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Entrez Id: 3046
Gene Symbol: HBE1
HBE1 		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: 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: 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: 3048
Gene Symbol: HBG2
HBG2 		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: 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: 282763
Gene Symbol: OR51B5
OR51B5 		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 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: 56547
Gene Symbol: MMP26
MMP26 		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: 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: 4163
Gene Symbol: MCC
MCC 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
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: 401662
Gene Symbol: OR51A8P
OR51A8P 		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: 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: 3042
Gene Symbol: HBM
HBM 		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: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype GWASCAT Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
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