rs756699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs756699(C;C) |
| Make rs756699(C;T) |
| Make rs756699(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 134110884 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs756699 |
| dbSNP (classic) | rs756699 |
| ClinGen | rs756699 |
| ebi | rs756699 |
| HLI | rs756699 |
| Exac | rs756699 |
| Gnomad | rs756699 |
| Varsome | rs756699 |
| LitVar | rs756699 |
| Map | rs756699 |
| PheGenI | rs756699 |
| Biobank | rs756699 |
| 1000 genomes | rs756699 |
| hgdp | rs756699 |
| ensembl | rs756699 |
| geneview | rs756699 |
| scholar | rs756699 |
| rs756699 | |
| pharmgkb | rs756699 |
| gwascentral | rs756699 |
| openSNP | rs756699 |
| 23andMe | rs756699 |
| SNPshot | rs756699 |
| SNPdbe | rs756699 |
| MSV3d | rs756699 |
| GWAS Ctlg | rs756699 |
| GMAF | 0.1961 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | A |
| P-val | 6E-7 |
| Odds Ratio | 1.1200 [1.10-1.14] |
[PMID 18045485] The candidate genes TAF5L, TCF7, PDCD1, IL6 and ICAM1 cannot be excluded from having effects in type 1 diabetes.
