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rs6292954

From SNPedia

Orientationplus
Stabilizedplus
Make rs6292954(G;G)
Make rs6292954(G;T)
Make rs6292954(T;T)
ReferenceGRCm38.p1 38.2/138
Chromosome12
Position9948200
is asnp
is mentioned by
dbSNPrs6292954
ebirs6292954
HLIrs6292954
Exacrs6292954
Varsomers6292954
Maprs6292954
PheGenIrs6292954
hapmaprs6292954
1000 genomesrs6292954
hgdprs6292954
ensemblrs6292954
gopubmedrs6292954
geneviewrs6292954
scholarrs6292954
googlers6292954
pharmgkbrs6292954
gwascentralrs6292954
openSNPrs6292954
23andMers6292954
23andMe allrs6292954
SNP Nexus

SNPshotrs6292954
SNPdbers6292954
MSV3drs6292954
GWAS Ctlgrs6292954
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