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rs4769060

From SNPedia

Orientationplus
Stabilizedplus
Make rs4769060(A;A)
Make rs4769060(A;G)
Make rs4769060(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position30763740
GeneALOX5AP
is asnp
is mentioned by
dbSNPrs4769060
ebirs4769060
HLIrs4769060
Exacrs4769060
Varsomers4769060
Maprs4769060
PheGenIrs4769060
hapmaprs4769060
1000 genomesrs4769060
hgdprs4769060
ensemblrs4769060
gopubmedrs4769060
geneviewrs4769060
scholarrs4769060
googlers4769060
pharmgkbrs4769060
gwascentralrs4769060
openSNPrs4769060
23andMers4769060
23andMe allrs4769060
SNP Nexus

SNPshotrs4769060
SNPdbers4769060
MSV3drs4769060
GWAS Ctlgrs4769060
GMAF0.3356
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 24225399] Genetic factors associated with gemcitabine pharmacokinetics, disposition, and toxicity


[PMID 24368493] Interaction between ALOX5AP and CYP3A5 gene variants significantly increases the risk for cerebral infarctions in Chinese


[PMID 24485247] Ischemic stroke risk in a southeastern Chinese population: Insights from 5-lipoxygenase activating protein and phosphodiesterase 4D single-nucleotide polymorphisms


[PMID 20592751OA-icon.png] Human lipoxygenase pathway gene variation and association with markers of subclinical atherosclerosis in the diabetes heart study.