rs1111875, None

N. diseases: 10
Disease: Impaired glucose tolerance ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
0.010 GeneticVariation BEFREE In this study, we asked whether the co-occurrence of risk alleles in or near five genes modulating insulin secretion (TCF7L2 rs7903146, IGF2BP2 rs4402960, CDKAL1 rs7754840, HHEX rs1111875, and HNF1A rs1169288) is associated with a higher risk of IGT/T2D in obese children and adolescents. 24062323 2014