|?|| (A;A) (A;T) (T;T) ||28|
This SNP, located in an intron of a gene (HNRPUL1
) on chromosome 19, may be associated with early onset myocardial infarction (MI). The risk allele for this SNP is the most common allele, rs11881940(A)
, with an odds ratio of 1.92 (1.28â€“2.86), and therefore it is also possible the view the rarer allele, rs11881940(T)
, as potentially playing a protective role against early onset MI. [PMID 16690874
[PMID 17767904] Genetic and genomic insights into the molecular basis of atherosclerosis.
[PMID 18599554] Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.
[PMID 24782050] Gene polymorphisms associated with susceptibility to coronary artery disease in Han Chinese people