rs7191888
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7191888(A;A) |
| Make rs7191888(A;G) |
| Make rs7191888(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 73547159 |
| Gene | C16orf47 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7191888 |
| dbSNP (classic) | rs7191888 |
| ClinGen | rs7191888 |
| ebi | rs7191888 |
| HLI | rs7191888 |
| Exac | rs7191888 |
| Gnomad | rs7191888 |
| Varsome | rs7191888 |
| LitVar | rs7191888 |
| Map | rs7191888 |
| PheGenI | rs7191888 |
| Biobank | rs7191888 |
| 1000 genomes | rs7191888 |
| hgdp | rs7191888 |
| ensembl | rs7191888 |
| geneview | rs7191888 |
| scholar | rs7191888 |
| rs7191888 | |
| pharmgkb | rs7191888 |
| gwascentral | rs7191888 |
| openSNP | rs7191888 |
| 23andMe | rs7191888 |
| SNPshot | rs7191888 |
| SNPdbe | rs7191888 |
| MSV3d | rs7191888 |
| GWAS Ctlg | rs7191888 |
| GMAF | 0.1878 |
| 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 |
