rs7191700
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7191700(C;C) |
| Make rs7191700(C;T) |
| Make rs7191700(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 11312946 |
| Gene | LOC105371082 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7191700 |
| dbSNP (classic) | rs7191700 |
| ClinGen | rs7191700 |
| ebi | rs7191700 |
| HLI | rs7191700 |
| Exac | rs7191700 |
| Gnomad | rs7191700 |
| Varsome | rs7191700 |
| LitVar | rs7191700 |
| Map | rs7191700 |
| PheGenI | rs7191700 |
| Biobank | rs7191700 |
| 1000 genomes | rs7191700 |
| hgdp | rs7191700 |
| ensembl | rs7191700 |
| geneview | rs7191700 |
| scholar | rs7191700 |
| rs7191700 | |
| pharmgkb | rs7191700 |
| gwascentral | rs7191700 |
| openSNP | rs7191700 |
| 23andMe | rs7191700 |
| SNPshot | rs7191700 |
| SNPdbe | rs7191700 |
| MSV3d | rs7191700 |
| GWAS Ctlg | rs7191700 |
| GMAF | 0.2089 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22190364 ]
|
| Trait | |
| Title | Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. |
| Risk Allele | C |
| P-val | 6E-7 |
| Odds Ratio | 1.1500 None |
