rs6196216
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6196216(A;A) |
| Make rs6196216(A;G) |
| Make rs6196216(G;G) |
| Reference | GRCm38.p1 38.2/138 |
| Chromosome | 17 |
| Position | 8970523 |
| Gene | Pde10a |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6196216 |
| dbSNP (classic) | rs6196216 |
| ClinGen | rs6196216 |
| ebi | rs6196216 |
| HLI | rs6196216 |
| Exac | rs6196216 |
| Gnomad | rs6196216 |
| Varsome | rs6196216 |
| LitVar | rs6196216 |
| Map | rs6196216 |
| PheGenI | rs6196216 |
| Biobank | rs6196216 |
| 1000 genomes | rs6196216 |
| hgdp | rs6196216 |
| ensembl | rs6196216 |
| geneview | rs6196216 |
| scholar | rs6196216 |
| rs6196216 | |
| pharmgkb | rs6196216 |
| gwascentral | rs6196216 |
| openSNP | rs6196216 |
| 23andMe | rs6196216 |
| SNPshot | rs6196216 |
| SNPdbe | rs6196216 |
| MSV3d | rs6196216 |
| GWAS Ctlg | rs6196216 |
| 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
