Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64478
Gene Symbol: CSMD1
CSMD1 		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 identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
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: 56547
Gene Symbol: MMP26
MMP26 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Entrez Id: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype GWASDB A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. 17767159 2007
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: 10767
Gene Symbol: HBS1L
HBS1L 		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: 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: 10767
Gene Symbol: HBS1L
HBS1L 		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: 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: 10767
Gene Symbol: HBS1L
HBS1L 		0.100 GeneticVariation phenotype GWASCAT A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. 17767159 2007
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: 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: 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: 3048
Gene Symbol: HBG2
HBG2 		0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
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: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype GWASCAT Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania. 25372704 2014
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L 		0.100 GeneticVariation phenotype GWASDB A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. 17767159 2007
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