rs1800777, CETP

N. diseases: 17
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
0.020 GeneticVariation BEFREE We identified a rare missense variant in CETP (cholesteryl ester transfer protein gene; rs1800777-A) that was associated with significant reductions in HDL-C levels during sepsis. 30321485 2019
Sepsis
CUI: C0243026
Disease: Sepsis
0.020 GeneticVariation BEFREE CETP genetic variant rs1800777 (allele A) is associated with abnormally low HDL-C levels and increased risk of AKI during sepsis. 30425299 2018