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rs4293222

From SNPedia

Orientationplus
Stabilizedplus
Make rs4293222(C;C)
Make rs4293222(C;G)
Make rs4293222(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position30737636
GeneALOX5AP
is asnp
is mentioned by
dbSNPrs4293222
ebirs4293222
HLIrs4293222
Exacrs4293222
Varsomers4293222
Maprs4293222
PheGenIrs4293222
hapmaprs4293222
1000 genomesrs4293222
hgdprs4293222
ensemblrs4293222
gopubmedrs4293222
geneviewrs4293222
scholarrs4293222
googlers4293222
pharmgkbrs4293222
gwascentralrs4293222
openSNPrs4293222
23andMers4293222
23andMe allrs4293222
SNP Nexus

SNPshotrs4293222
SNPdbers4293222
MSV3drs4293222
GWAS Ctlgrs4293222
GMAF0.4715
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22051033] ALOX5AP genetic variants and risk of atherothrombotic stroke in the Taiwanese population


[PMID 18366797OA-icon.png] Influence of leukotriene gene polymorphisms on chronic rhinosinusitis.