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rs17222842

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17222842(A;A)
Make rs17222842(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position30765980
GeneALOX5AP
is asnp
is mentioned by
dbSNPrs17222842
ebirs17222842
HLIrs17222842
Exacrs17222842
Varsomers17222842
Maprs17222842
PheGenIrs17222842
hapmaprs17222842
1000 genomesrs17222842
hgdprs17222842
ensemblrs17222842
gopubmedrs17222842
geneviewrs17222842
scholarrs17222842
googlers17222842
pharmgkbrs17222842
gwascentralrs17222842
openSNPrs17222842
23andMers17222842
23andMe allrs17222842
SNP Nexus

SNPshotrs17222842
SNPdbers17222842
MSV3drs17222842
GWAS Ctlgrs17222842
GMAF0.03857
Max Magnitude0
rs17222842, also known as SG13S35, is an ALOX5AP gene SNP that has been defined as part of a haplotype potentially associated with risk for myocardial infarction or ischemic stroke. Details of this haplotype and several related studies are on the ALOX5AP page.


[PMID 19130089OA-icon.png] Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.


[PMID 19361804] 5-Lipoxygenase activating protein (ALOX5AP) gene variants associate with the presence of xanthomas in familial hypercholesterolemia.


[PMID 19751821OA-icon.png] Oxidative risk for atherothrombotic cardiovascular disease.


[PMID 27893808] Common Polymorphisms in the 5-Lipoxygenase Pathway and Risk of Incident Myocardial Infarction: A Danish Case-Cohort Study.