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rs5628

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs5628(C;T)
Make rs5628(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position49524145
GenePTGIS
is asnp
is mentioned by
dbSNPrs5628
ebirs5628
HLIrs5628
Exacrs5628
Varsomers5628
Maprs5628
PheGenIrs5628
hapmaprs5628
1000 genomesrs5628
hgdprs5628
ensemblrs5628
gopubmedrs5628
geneviewrs5628
scholarrs5628
googlers5628
pharmgkbrs5628
gwascentralrs5628
openSNPrs5628
23andMers5628
23andMe allrs5628
SNP Nexus

SNPshotrs5628
SNPdbers5628
MSV3drs5628
GWAS Ctlgrs5628
GMAF0.1047
Max Magnitude0
? (C;C) (C;T) (T;T) 28


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


[PMID 19046748OA-icon.png] Variation in eicosanoid genes, non-fatal myocardial infarction and ischemic stroke.


GET Evidence
rs5628
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0934189
summary