rs11129295
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11129295(C;C) |
| Make rs11129295(C;T) |
| Make rs11129295(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 27747289 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11129295 |
| dbSNP (classic) | rs11129295 |
| ClinGen | rs11129295 |
| ebi | rs11129295 |
| HLI | rs11129295 |
| Exac | rs11129295 |
| Gnomad | rs11129295 |
| Varsome | rs11129295 |
| LitVar | rs11129295 |
| Map | rs11129295 |
| PheGenI | rs11129295 |
| Biobank | rs11129295 |
| 1000 genomes | rs11129295 |
| hgdp | rs11129295 |
| ensembl | rs11129295 |
| geneview | rs11129295 |
| scholar | rs11129295 |
| rs11129295 | |
| pharmgkb | rs11129295 |
| gwascentral | rs11129295 |
| openSNP | rs11129295 |
| 23andMe | rs11129295 |
| SNPshot | rs11129295 |
| SNPdbe | rs11129295 |
| MSV3d | rs11129295 |
| GWAS Ctlg | rs11129295 |
| GMAF | 0.494 |
| 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 | 1E-9 |
| Odds Ratio | 1.1100 [1.09-1.12] |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 3
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
