Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3191333
rs3191333
0.010 GeneticVariation BEFREE <b>Results:</b> Our findings show that a <i>KLF4</i> genomic variant (rs2236599) is associated with HU treatment efficacy in sickle cell disease/β-thalassemia compound heterozygous patients and two <i>KLF10</i> genomic variants (rs980112, rs3191333) are associated with persistent HbF levels in NTDT patients. 31393228

2019