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rs6538697

From SNPedia

Orientationplus
Stabilizedplus
Make rs6538697(C;C)
Make rs6538697(C;T)
Make rs6538697(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position96009832
GeneLTA4H
is asnp
is mentioned by
dbSNPrs6538697
ebirs6538697
HLIrs6538697
Exacrs6538697
Varsomers6538697
Maprs6538697
PheGenIrs6538697
hapmaprs6538697
1000 genomesrs6538697
hgdprs6538697
ensemblrs6538697
gopubmedrs6538697
geneviewrs6538697
scholarrs6538697
googlers6538697
pharmgkbrs6538697
gwascentralrs6538697
openSNPrs6538697
23andMers6538697
23andMe allrs6538697
SNP Nexus

SNPshotrs6538697
SNPdbers6538697
MSV3drs6538697
GWAS Ctlgrs6538697
GMAF0.1671
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23079278] Genetic variation in members of the leukotrienes biosynthesis pathway confers risk of ischemic stroke in Eastern Han Chinese


[PMID 23324273] Association between genetic variants of the leukotriene biosynthesis pathway and the risk of stroke: a case-control study in the Chinese Han population


[PMID 19130089OA-icon.png] Genetic effects in the leukotriene biosynthesis pathway and association with atherosclerosis.


[PMID 25721704] Variants in ALOX5, ALOX5AP and LTA4H are not associated with atherosclerotic plaque phenotypes: The Athero-Express Genomics Study