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rs9315050

From SNPedia

Orientationplus
Stabilizedplus
Make rs9315050(A;A)
Make rs9315050(A;G)
Make rs9315050(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position30761908
GeneALOX5AP
is asnp
is mentioned by
dbSNPrs9315050
ebirs9315050
HLIrs9315050
Exacrs9315050
Varsomers9315050
Maprs9315050
PheGenIrs9315050
hapmaprs9315050
1000 genomesrs9315050
hgdprs9315050
ensemblrs9315050
gopubmedrs9315050
geneviewrs9315050
scholarrs9315050
googlers9315050
pharmgkbrs9315050
gwascentralrs9315050
openSNPrs9315050
23andMers9315050
23andMe allrs9315050
SNP Nexus

SNPshotrs9315050
SNPdbers9315050
MSV3drs9315050
GWAS Ctlgrs9315050
GMAF0.0978
Max Magnitude
? (A;A) (A;G) (G;G) 28
rs9315050, also known as SG13S41, 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 19665766OA-icon.png] Genetics and pharmacogenetics of the leukotriene pathway.


[PMID 26885075] A tagging ALOX5AP polymorphism and risk of ischemic stroke in a northeastern Chinese Han population.