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rs2228064

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2228064(A;A)
Make rs2228064(A;G)
ReferenceGRCh37.p5 37.3/135
Chromosome10
Position45878050
GeneALOX5
is asnp
is mentioned by
dbSNPrs2228064
ebirs2228064
HLIrs2228064
Exacrs2228064
Varsomers2228064
Maprs2228064
PheGenIrs2228064
hapmaprs2228064
1000 genomesrs2228064
hgdprs2228064
ensemblrs2228064
gopubmedrs2228064
geneviewrs2228064
scholarrs2228064
googlers2228064
pharmgkbrs2228064
gwascentralrs2228064
openSNPrs2228064
23andMers2228064
23andMe allrs2228064
SNP Nexus

SNPshotrs2228064
SNPdbers2228064
MSV3drs2228064
GWAS Ctlgrs2228064
GMAF0.1019
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 21816595] A Promoter polymorphism (rs17222919, -1316T/G) of ALOX5AP is associated with intracerebral hemorrhage in Korean population


[PMID 18248681OA-icon.png] Prevalence of common disease-associated variants in Asian Indians.