rs10259085
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10259085(C;C) |
| Make rs10259085(C;T) |
| Make rs10259085(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 7228800 |
| Gene | C1GALT1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10259085 |
| dbSNP (classic) | rs10259085 |
| ClinGen | rs10259085 |
| ebi | rs10259085 |
| HLI | rs10259085 |
| Exac | rs10259085 |
| Gnomad | rs10259085 |
| Varsome | rs10259085 |
| LitVar | rs10259085 |
| Map | rs10259085 |
| PheGenI | rs10259085 |
| Biobank | rs10259085 |
| 1000 genomes | rs10259085 |
| hgdp | rs10259085 |
| ensembl | rs10259085 |
| geneview | rs10259085 |
| scholar | rs10259085 |
| rs10259085 | |
| pharmgkb | rs10259085 |
| gwascentral | rs10259085 |
| openSNP | rs10259085 |
| 23andMe | rs10259085 |
| SNPshot | rs10259085 |
| SNPdbe | rs10259085 |
| MSV3d | rs10259085 |
| GWAS Ctlg | rs10259085 |
| GMAF | 0.4017 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 0.000004 |
| Odds Ratio | NR NR |
