rs1360485, HMGB1

N. diseases: 16
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Sepsis
CUI: C0243026
Disease: Sepsis
0.010 GeneticVariation BEFREE The HMGB1 gene rs2249825 and rs1045411 site SNPs were associated with sepsis risk, but the rs1360485 site SNP was not associated with sepsis risk. 30423384 2019