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rs11881940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) normal form
(A;T) 1.9x risk of MI
(T;T) 1.9x risk of MI
ReferenceGRCh38 38.1/141
Chromosome19
Position41302527
GeneHNRNPUL1
is asnp
is mentioned by
dbSNPrs11881940
ebirs11881940
HLIrs11881940
Exacrs11881940
Varsomers11881940
Maprs11881940
PheGenIrs11881940
hapmaprs11881940
1000 genomesrs11881940
hgdprs11881940
ensemblrs11881940
gopubmedrs11881940
geneviewrs11881940
scholarrs11881940
googlers11881940
pharmgkbrs11881940
gwascentralrs11881940
openSNPrs11881940
23andMers11881940
23andMe allrs11881940
SNP Nexus

SNPshotrs11881940
SNPdbers11881940
MSV3drs11881940
GWAS Ctlgrs11881940
GMAF0.1662
Max Magnitude
? (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 (1.28–2.86), 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 17767904OA-icon.png] Genetic and genomic insights into the molecular basis of atherosclerosis.


[PMID 18599554OA-icon.png] 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