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rs13481324

From SNPedia

Orientationplus
Stabilizedplus
Make rs13481324(C;C)
Make rs13481324(C;T)
Make rs13481324(T;T)
ReferenceGRCm38.p1 38.2/138
Chromosome12
Position17574544
is asnp
is mentioned by
dbSNPrs13481324
ebirs13481324
HLIrs13481324
Exacrs13481324
Varsomers13481324
Maprs13481324
PheGenIrs13481324
hapmaprs13481324
1000 genomesrs13481324
hgdprs13481324
ensemblrs13481324
gopubmedrs13481324
geneviewrs13481324
scholarrs13481324
googlers13481324
pharmgkbrs13481324
gwascentralrs13481324
openSNPrs13481324
23andMers13481324
23andMe allrs13481324
SNP Nexus

SNPshotrs13481324
SNPdbers13481324
MSV3drs13481324
GWAS Ctlgrs13481324
Max Magnitude

[PMID 24090483OA-icon.png] Quantitative trait loci analysis reveals candidate genes implicated in regulating functional deficit and CNS vascular permeability in CD8 T cell-initiated blood--brain barrier disruption