rs7606173, BCL11A

N. diseases: 5
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
0.800 GeneticVariation GWASCAT Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Fetal hemoglobin determination
CUI: C0200695
Disease: Fetal hemoglobin determination
0.800 GeneticVariation GWASDB Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
Red cell distribution width determination
0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
Red cell distribution width determination
0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
RDW - Red blood cell distribution width result
0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
Anemia, Sickle Cell
CUI: C0002895
Disease: Anemia, Sickle Cell
0.700 GeneticVariation GWASCAT Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. 21326311 2011
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
0.700 GeneticVariation GWASDB Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. 19862010 2009