rs6659742
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6659742(C;C) |
| Make rs6659742(C;T) |
| Make rs6659742(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 159848723 |
| Gene | C1orf204 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6659742 |
| dbSNP (classic) | rs6659742 |
| ClinGen | rs6659742 |
| ebi | rs6659742 |
| HLI | rs6659742 |
| Exac | rs6659742 |
| Gnomad | rs6659742 |
| Varsome | rs6659742 |
| LitVar | rs6659742 |
| Map | rs6659742 |
| PheGenI | rs6659742 |
| Biobank | rs6659742 |
| 1000 genomes | rs6659742 |
| hgdp | rs6659742 |
| ensembl | rs6659742 |
| geneview | rs6659742 |
| scholar | rs6659742 |
| rs6659742 | |
| pharmgkb | rs6659742 |
| gwascentral | rs6659742 |
| openSNP | rs6659742 |
| 23andMe | rs6659742 |
| SNPshot | rs6659742 |
| SNPdbe | rs6659742 |
| MSV3d | rs6659742 |
| GWAS Ctlg | rs6659742 |
| GMAF | 0.3691 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23472185 ]
|
| Trait | Multiple sclerosis (OCB status) |
| Title | Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. |
| Risk Allele | |
| P-val | 7E-7 |
| Odds Ratio | 1.99 [1.52-2.61] |
