rs929156
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs929156(C;C) |
| Make rs929156(C;T) |
| Make rs929156(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 30171922 |
| Gene | TRIM15 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs929156 |
| dbSNP (classic) | rs929156 |
| ClinGen | rs929156 |
| ebi | rs929156 |
| HLI | rs929156 |
| Exac | rs929156 |
| Gnomad | rs929156 |
| Varsome | rs929156 |
| LitVar | rs929156 |
| Map | rs929156 |
| PheGenI | rs929156 |
| Biobank | rs929156 |
| 1000 genomes | rs929156 |
| hgdp | rs929156 |
| ensembl | rs929156 |
| geneview | rs929156 |
| scholar | rs929156 |
| rs929156 | |
| pharmgkb | rs929156 |
| gwascentral | rs929156 |
| openSNP | rs929156 |
| 23andMe | rs929156 |
| SNPshot | rs929156 |
| SNPdbe | rs929156 |
| MSV3d | rs929156 |
| GWAS Ctlg | rs929156 |
| GMAF | 0.2006 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19010793
] Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
