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rs7291467

From SNPedia

Orientationplus
Stabilizedplus
Make rs7291467(A;A)
Make rs7291467(A;G)
Make rs7291467(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37576621
GeneLGALS2, LOC100652769
is asnp
is mentioned by
dbSNPrs7291467
ebirs7291467
HLIrs7291467
Exacrs7291467
Varsomers7291467
Maprs7291467
PheGenIrs7291467
hapmaprs7291467
1000 genomesrs7291467
hgdprs7291467
ensemblrs7291467
gopubmedrs7291467
geneviewrs7291467
scholarrs7291467
googlers7291467
pharmgkbrs7291467
gwascentralrs7291467
openSNPrs7291467
23andMers7291467
23andMe allrs7291467
SNP Nexus

SNPshotrs7291467
SNPdbers7291467
MSV3drs7291467
GWAS Ctlgrs7291467
GMAF0.4389
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20500087OA-icon.png] Age-Related Susceptibility to Severe Malaria Associated with Galectin-2 in Highland Papuans


[PMID 22310064] Polymorphisms of LTA, LGALS2, and PSMA6 genes and coronary atherosclerosis: a pathological study of 1503 consecutive autopsy cases


[PMID 16468038] Genotype of galectin 2 (LGALS2) is associated with insulin-glucose profile in the British Women's Heart and Health Study.


[PMID 17098239] LGALS2 functional variant rs7291467 is not associated with susceptibility to myocardial infarction in Caucasians.


[PMID 17517687] Association of variants in the BAT1-NFKBIL1-LTA genomic region with protection against myocardial infarction in Europeans.


[PMID 17767904OA-icon.png] Genetic and genomic insights into the molecular basis of atherosclerosis.


[PMID 18506375] Association of genetic variants with atherothrombotic cerebral infarction in Japanese individuals with metabolic syndrome.


[PMID 21831908] Galectin-2 expression is dependent on the rs7291467 polymorphism and acts as an inhibitor of arteriogenesis.

Coronary Heart Disease