Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6037828
rs6037828
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
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