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rs5629

From SNPedia

Orientationminus
Stabilizedminus
Make rs5629(A;A)
Make rs5629(A;C)
Make rs5629(C;C)
ReferenceGRCh38 38.1/141
Chromosome20
Position49513169
GenePTGIS
is asnp
is mentioned by
dbSNPrs5629
ebirs5629
HLIrs5629
Exacrs5629
Varsomers5629
Maprs5629
PheGenIrs5629
hapmaprs5629
1000 genomesrs5629
hgdprs5629
ensemblrs5629
gopubmedrs5629
geneviewrs5629
scholarrs5629
googlers5629
pharmgkbrs5629
gwascentralrs5629
openSNPrs5629
23andMers5629
23andMe allrs5629
SNP Nexus

SNPshotrs5629
SNPdbers5629
MSV3drs5629
GWAS Ctlgrs5629
GMAF0.2222
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 19719985] Resequencing and association study of vesicular glutamate transporter 1 gene (VGLUT1) with schizophrenia



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


[PMID 19147528] Haplotype analysis of the CYP8A1 gene associated with myocardial infarction.


GET Evidence
rs5629
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.218442
summary