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 GWASCAT Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. 27022141 2016
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: 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: 3048
Gene Symbol: HBG2
HBG2
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 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 Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania. 25372704 2014
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: 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: 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: 53335
Gene Symbol: BCL11A
BCL11A
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: 3048
Gene Symbol: HBG2
HBG2
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: 282763
Gene Symbol: OR51B5
OR51B5
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: 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: 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: 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: 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: 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: 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: 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: 3046
Gene Symbol: HBE1
HBE1
0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Entrez Id: 282763
Gene Symbol: OR51B5
OR51B5
0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Entrez Id: 4163
Gene Symbol: MCC
MCC
0.100 GeneticVariation phenotype GWASCAT Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Entrez Id: 10767
Gene Symbol: HBS1L
HBS1L
0.100 GeneticVariation phenotype GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
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