Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: 3048
Gene Symbol: HBG2
HBG2 		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: 100616473
Gene Symbol: MIR4432
MIR4432 		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: 53335
Gene Symbol: BCL11A
BCL11A 		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: 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: 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: 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: 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: 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: 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