rs1800625, AGER;PBX2

N. diseases: 39
Disease: Sepsis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sepsis
CUI: C0243026
Disease: Sepsis
0.030 GeneticVariation BEFREE Significant differences were observed in the rs1800624 and rs1800625 genotype/allele distributions between the sepsis and controls, but no significant difference was observed in the rs2070600 genotype/allele. 27172264 2017
Sepsis
CUI: C0243026
Disease: Sepsis
0.030 GeneticVariation BEFREE The rs1800625 polymorphism is a functional single nucleotide polymorphism and confers host susceptibility to sepsis and MODS in patients with major trauma. 25572180 2015
Sepsis
CUI: C0243026
Disease: Sepsis
0.030 GeneticVariation BEFREE The rs1800625 polymorphism is a functional variant, which might be used as a relevant risk estimate for the development of sepsis and multiple organ dysfunction syndrome in patients with major trauma. 22827914 2012