rs2283792
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2283792(G;G) |
| Make rs2283792(G;T) |
| Make rs2283792(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 21776836 |
| Gene | MAPK1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2283792 |
| dbSNP (classic) | rs2283792 |
| ClinGen | rs2283792 |
| ebi | rs2283792 |
| HLI | rs2283792 |
| Exac | rs2283792 |
| Gnomad | rs2283792 |
| Varsome | rs2283792 |
| LitVar | rs2283792 |
| Map | rs2283792 |
| PheGenI | rs2283792 |
| Biobank | rs2283792 |
| 1000 genomes | rs2283792 |
| hgdp | rs2283792 |
| ensembl | rs2283792 |
| geneview | rs2283792 |
| scholar | rs2283792 |
| rs2283792 | |
| pharmgkb | rs2283792 |
| gwascentral | rs2283792 |
| openSNP | rs2283792 |
| 23andMe | rs2283792 |
| SNPshot | rs2283792 |
| SNPdbe | rs2283792 |
| MSV3d | rs2283792 |
| GWAS Ctlg | rs2283792 |
| GMAF | 0.4591 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | C |
| P-val | 5E-9 |
| Odds Ratio | 1.1000 [1.08-1.11] |
[PMID 17357082] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
