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rs13481303

From SNPedia

Orientationplus
Stabilizedplus
Make rs13481303(A;A)
Make rs13481303(A;C)
Make rs13481303(C;C)
ReferenceGRCm38.p1 38.2/138
Chromosome12
Position11915327
is asnp
is mentioned by
dbSNPrs13481303
ebirs13481303
HLIrs13481303
Exacrs13481303
Varsomers13481303
Maprs13481303
PheGenIrs13481303
hapmaprs13481303
1000 genomesrs13481303
hgdprs13481303
ensemblrs13481303
gopubmedrs13481303
geneviewrs13481303
scholarrs13481303
googlers13481303
pharmgkbrs13481303
gwascentralrs13481303
openSNPrs13481303
23andMers13481303
23andMe allrs13481303
SNP Nexus

SNPshotrs13481303
SNPdbers13481303
MSV3drs13481303
GWAS Ctlgrs13481303
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