Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11037444
rs11037444
Entrez Id: 3046;3048;282763;390063
Gene Symbol: HBE1;HBG2;OR51B5;OR51I1
HBE1;HBG2;OR51B5;OR51I1
CUI: C0200695
Disease:
Fetal hemoglobin determination
0.700 GeneticVariation GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008