rs874628
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs874628(C;C) |
| Make rs874628(C;T) |
| Make rs874628(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 18193890 |
| Gene | MPV17L2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs874628 |
| dbSNP (classic) | rs874628 |
| ClinGen | rs874628 |
| ebi | rs874628 |
| HLI | rs874628 |
| Exac | rs874628 |
| Gnomad | rs874628 |
| Varsome | rs874628 |
| LitVar | rs874628 |
| Map | rs874628 |
| PheGenI | rs874628 |
| Biobank | rs874628 |
| 1000 genomes | rs874628 |
| hgdp | rs874628 |
| ensembl | rs874628 |
| geneview | rs874628 |
| scholar | rs874628 |
| rs874628 | |
| pharmgkb | rs874628 |
| gwascentral | rs874628 |
| openSNP | rs874628 |
| 23andMe | rs874628 |
| SNPshot | rs874628 |
| SNPdbe | rs874628 |
| MSV3d | rs874628 |
| GWAS Ctlg | rs874628 |
| GMAF | 0.1919 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | A |
| P-val | 1E-8 |
| Odds Ratio | 1.1100 [1.09-1.12] |
[PMID 15752431] Association between a variation in the phosphodiesterase 4D gene and bone mineral density.
[PMID 16584842] Variants in the RAB3A gene are not associated with mental retardation in the Chinese population.
[PMID 20405052] The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.
