{{Rsnum
|rsid=11881940
|Gene=HNRNPUL1
|Chromosome=19
|position=41302527
|Orientation=plus
|GMAF=0.1662
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene_s=HNRNPUL1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 76.9 | 23.1 | 0.0
| HCB | 59.5 | 26.2 | 14.3
| JPT | 71.1 | 28.9 | 0.0
| YRI | 87.1 | 12.9 | 0.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 59.5 | 26.2 | 14.3
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=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 Auto
|PMID=17767904
|Title=Genetic and genomic insights into the molecular basis of atherosclerosis.
|OA=1
}}

{{PMID Auto
|PMID=18599554
|Title=Replication study of 10 genetic polymorphisms associated with coronary heart disease in a specific high-risk population with familial hypercholesterolemia.
|OA=1
}}

{{PMID Auto
|PMID=24782050
|Title=Gene polymorphisms associated with susceptibility to coronary artery disease in Han Chinese people
}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}