rs3655057
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3655057(A;A) |
| Make rs3655057(A;G) |
| Make rs3655057(G;G) |
| Reference | GRCm38.p1 38.2/138 |
| Chromosome | 12 |
| Position | 13383077 |
| Gene | Nbas |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3655057 |
| dbSNP (classic) | rs3655057 |
| ClinGen | rs3655057 |
| ebi | rs3655057 |
| HLI | rs3655057 |
| Exac | rs3655057 |
| Gnomad | rs3655057 |
| Varsome | rs3655057 |
| LitVar | rs3655057 |
| Map | rs3655057 |
| PheGenI | rs3655057 |
| Biobank | rs3655057 |
| 1000 genomes | rs3655057 |
| hgdp | rs3655057 |
| ensembl | rs3655057 |
| geneview | rs3655057 |
| scholar | rs3655057 |
| rs3655057 | |
| pharmgkb | rs3655057 |
| gwascentral | rs3655057 |
| openSNP | rs3655057 |
| 23andMe | rs3655057 |
| SNPshot | rs3655057 |
| SNPdbe | rs3655057 |
| MSV3d | rs3655057 |
| GWAS Ctlg | rs3655057 |
| 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
