rs3672065
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3672065(C;C) |
Make rs3672065(C;T) |
Make rs3672065(T;T) |
Reference | GRCm38.p1 38.2/138 |
Chromosome | 17 |
Position | 14199394 |
Gene | Dact2 |
is a | snp |
is | mentioned by |
dbSNP | rs3672065 |
dbSNP (classic) | rs3672065 |
ClinGen | rs3672065 |
ebi | rs3672065 |
HLI | rs3672065 |
Exac | rs3672065 |
Gnomad | rs3672065 |
Varsome | rs3672065 |
LitVar | rs3672065 |
Map | rs3672065 |
PheGenI | rs3672065 |
Biobank | rs3672065 |
1000 genomes | rs3672065 |
hgdp | rs3672065 |
ensembl | rs3672065 |
geneview | rs3672065 |
scholar | rs3672065 |
rs3672065 | |
pharmgkb | rs3672065 |
gwascentral | rs3672065 |
openSNP | rs3672065 |
23andMe | rs3672065 |
SNPshot | rs3672065 |
SNPdbe | rs3672065 |
MSV3d | rs3672065 |
GWAS Ctlg | rs3672065 |
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