rs2116078
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2116078(G;G) |
| Make rs2116078(G;T) |
| Make rs2116078(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 72451754 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2116078 |
| dbSNP (classic) | rs2116078 |
| ClinGen | rs2116078 |
| ebi | rs2116078 |
| HLI | rs2116078 |
| Exac | rs2116078 |
| Gnomad | rs2116078 |
| Varsome | rs2116078 |
| LitVar | rs2116078 |
| Map | rs2116078 |
| PheGenI | rs2116078 |
| Biobank | rs2116078 |
| 1000 genomes | rs2116078 |
| hgdp | rs2116078 |
| ensembl | rs2116078 |
| geneview | rs2116078 |
| scholar | rs2116078 |
| rs2116078 | |
| pharmgkb | rs2116078 |
| gwascentral | rs2116078 |
| openSNP | rs2116078 |
| 23andMe | rs2116078 |
| SNPshot | rs2116078 |
| SNPdbe | rs2116078 |
| MSV3d | rs2116078 |
| GWAS Ctlg | rs2116078 |
| GMAF | 0.3903 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 19010793 ]
|
| Trait | Multiple sclerosis (age of onset) |
| Title | Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | NR NR |
