rs180358
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs180358(A;A) |
| Make rs180358(A;G) |
| Make rs180358(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 11 |
| Position | 116728676 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs180358 |
| dbSNP (classic) | rs180358 |
| ClinGen | rs180358 |
| ebi | rs180358 |
| HLI | rs180358 |
| Exac | rs180358 |
| Gnomad | rs180358 |
| Varsome | rs180358 |
| LitVar | rs180358 |
| Map | rs180358 |
| PheGenI | rs180358 |
| Biobank | rs180358 |
| 1000 genomes | rs180358 |
| hgdp | rs180358 |
| ensembl | rs180358 |
| geneview | rs180358 |
| scholar | rs180358 |
| rs180358 | |
| pharmgkb | rs180358 |
| gwascentral | rs180358 |
| openSNP | rs180358 |
| 23andMe | rs180358 |
| SNPshot | rs180358 |
| SNPdbe | rs180358 |
| MSV3d | rs180358 |
| GWAS Ctlg | rs180358 |
| GMAF | 0.1419 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis (severity) |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | NR NR |
