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rs3655057

From SNPedia

Orientationplus
Stabilizedplus
Make rs3655057(A;A)
Make rs3655057(A;G)
Make rs3655057(G;G)
ReferenceGRCm38.p1 38.2/138
Chromosome12
Position13383077
GeneNbas
is asnp
is mentioned by
dbSNPrs3655057
ebirs3655057
HLIrs3655057
Exacrs3655057
Varsomers3655057
Maprs3655057
PheGenIrs3655057
hapmaprs3655057
1000 genomesrs3655057
hgdprs3655057
ensemblrs3655057
gopubmedrs3655057
geneviewrs3655057
scholarrs3655057
googlers3655057
pharmgkbrs3655057
gwascentralrs3655057
openSNPrs3655057
23andMers3655057
23andMe allrs3655057
SNP Nexus

SNPshotrs3655057
SNPdbers3655057
MSV3drs3655057
GWAS Ctlgrs3655057
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