rs17411949
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 |
| Make rs17411949(C;T) |
| Make rs17411949(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 140380851 |
| Gene | CLSTN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17411949 |
| dbSNP (classic) | rs17411949 |
| ClinGen | rs17411949 |
| ebi | rs17411949 |
| HLI | rs17411949 |
| Exac | rs17411949 |
| Gnomad | rs17411949 |
| Varsome | rs17411949 |
| LitVar | rs17411949 |
| Map | rs17411949 |
| PheGenI | rs17411949 |
| Biobank | rs17411949 |
| 1000 genomes | rs17411949 |
| hgdp | rs17411949 |
| ensembl | rs17411949 |
| geneview | rs17411949 |
| scholar | rs17411949 |
| rs17411949 | |
| pharmgkb | rs17411949 |
| gwascentral | rs17411949 |
| openSNP | rs17411949 |
| 23andMe | rs17411949 |
| SNPshot | rs17411949 |
| SNPdbe | rs17411949 |
| MSV3d | rs17411949 |
| GWAS Ctlg | rs17411949 |
| GMAF | 0.04591 |
| 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 | 8E-7 |
| Odds Ratio | 1.85 [1.45-2.37] |
