Source: GWASDB

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 390058
Gene Symbol: OR51B6
OR51B6
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.100 GeneticVariation 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
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.100 GeneticVariation 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
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		0.100 GeneticVariation GWASDB Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. 20018918

2010