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rs9579646

From SNPedia

Orientationplus
Stabilizedplus
Make rs9579646(A;A)
Make rs9579646(A;G)
Make rs9579646(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position30736442
GeneALOX5AP
is asnp
is mentioned by
dbSNPrs9579646
ebirs9579646
HLIrs9579646
Exacrs9579646
Varsomers9579646
Maprs9579646
PheGenIrs9579646
hapmaprs9579646
1000 genomesrs9579646
hgdprs9579646
ensemblrs9579646
gopubmedrs9579646
geneviewrs9579646
scholarrs9579646
googlers9579646
pharmgkbrs9579646
gwascentralrs9579646
openSNPrs9579646
23andMers9579646
23andMe allrs9579646
SNP Nexus

SNPshotrs9579646
SNPdbers9579646
MSV3drs9579646
GWAS Ctlgrs9579646
GMAF0.4931
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21153769] A tagging SNP in ALOX5AP and risk of stroke: a haplotype-based analysis among eastern Chinese Han population

[PMID 17387518] Association of ALOX5AP with ischemic stroke: a population-based case-control study.


[PMID 25902778] Impact of inflammation, gene variants, and cigarette smoking on coronary artery disease risk


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


[PMID 27416969] Genetic Variants in the Transcriptional Regulatory Region of the ALOX5AP gene and Susceptibility to Ischemic Stroke in Chinese Populations.