Fetal hemoglobin levels Gene Set

Dataset GWAS Catalog SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A fetal hemoglobin measurement is the quantification of fetal hemoglobin typically measured in the blood of children for diagnosis of congenital disease. (Experimental Factor Ontology, EFO_0004576)
External Link https://www.ebi.ac.uk/gwas/search?query=Fetal hemoglobin levels
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Genes

3 genes associated with the Fetal hemoglobin levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
BCL11A B-cell CLL/lymphoma 11A (zinc finger protein) 1.34418
LCRB locus control region, beta 1.09169
OR51B6 olfactory receptor, family 51, subfamily B, member 6 0.389385