rs13481303
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13481303(A;A) |
Make rs13481303(A;C) |
Make rs13481303(C;C) |
Reference | GRCm38.p1 38.2/138 |
Chromosome | 12 |
Position | 11915327 |
is a | snp |
is | mentioned by |
dbSNP | rs13481303 |
dbSNP (classic) | rs13481303 |
ClinGen | rs13481303 |
ebi | rs13481303 |
HLI | rs13481303 |
Exac | rs13481303 |
Gnomad | rs13481303 |
Varsome | rs13481303 |
LitVar | rs13481303 |
Map | rs13481303 |
PheGenI | rs13481303 |
Biobank | rs13481303 |
1000 genomes | rs13481303 |
hgdp | rs13481303 |
ensembl | rs13481303 |
geneview | rs13481303 |
scholar | rs13481303 |
rs13481303 | |
pharmgkb | rs13481303 |
gwascentral | rs13481303 |
openSNP | rs13481303 |
23andMe | rs13481303 |
SNPshot | rs13481303 |
SNPdbe | rs13481303 |
MSV3d | rs13481303 |
GWAS Ctlg | rs13481303 |
Max Magnitude | 0 |
[PMID 24090483] 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