|?|| (C;C) (C;T) (T;T) ||28|
|| [PMID 20864672]
|| Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
| Risk Allele
| Odds Ratio
|| 0.05 [0.04-0.06] unit decrease
[PMID 18439548] Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.
[PMID 18439552] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.
[PMID 23832694] Common genetic variants associated with lipid profiles in a Chinese pediatric population.