rs11466314
From SNPedia
					| Orientation | minus | 
| Stabilized | minus | 
| Geno | Mag | Summary | 
|---|---|---|
| (G;G) | 0 | common in complete genomics | 
| Make rs11466314(A;A) | 
| Make rs11466314(A;G) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 19 | 
| Position | 41354331 | 
| Gene | B9D2, TGFB1 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs11466314 | 
| dbSNP (classic) | rs11466314 | 
| ClinGen | rs11466314 | 
| ebi | rs11466314 | 
| HLI | rs11466314 | 
| Exac | rs11466314 | 
| Gnomad | rs11466314 | 
| Varsome | rs11466314 | 
| LitVar | rs11466314 | 
| Map | rs11466314 | 
| PheGenI | rs11466314 | 
| Biobank | rs11466314 | 
| 1000 genomes | rs11466314 | 
| hgdp | rs11466314 | 
| ensembl | rs11466314 | 
| geneview | rs11466314 | 
| scholar | rs11466314 | 
| rs11466314 | |
| pharmgkb | rs11466314 | 
| gwascentral | rs11466314 | 
| openSNP | rs11466314 | 
| 23andMe | rs11466314 | 
| SNPshot | rs11466314 | 
| SNPdbe | rs11466314 | 
| MSV3d | rs11466314 | 
| GWAS Ctlg | rs11466314 | 
| GMAF | 0.003214 | 
| Max Magnitude | 0 | 
[PMID 18366677
] Genes implicated in multiple sclerosis pathogenesis from consilience of genotyping and expression profiles in relapse and remission.
