rs780094, GCKR

N. diseases: 62
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
0.730 GeneticVariation GWASCAT A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia. 27599772 2017
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
0.730 GeneticVariation BEFREE The T2D risk alleles of rs972283 near KLF14 and rs11634397 near ZFAND6 were associated with a higher risk for elevated triglycerides (rs972283: 1.11 (1.02, 1.24), P = 1.46 × 10-2; rs11634397: 1.14 (1.00, 1.29), P = 4.66 × 10-2), while the T2D risk alleles of rs780094 in GCKR and rs7903146 in TCF7L2 were related to a lower risk of elevated triglycerides (rs780094: 0.86 (0.80, 0.93), P = 1.35 × 10-4; rs7903146: 0.82 (0.69, 0.98), P = 3.18 × 10-2). 26599349 2015
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
0.730 GeneticVariation BEFREE GCKR rs780094 was also associated with decreased plasma glucose, and increased triglycerides in the patient and control groups. 24785259 2014
Hypertriglyceridemia
CUI: C0020557
Disease: Hypertriglyceridemia
0.730 GeneticVariation BEFREE The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population. 20574426 2010