rs17066096
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17066096(A;A) |
| Make rs17066096(A;G) |
| Make rs17066096(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 137131771 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17066096 |
| dbSNP (classic) | rs17066096 |
| ClinGen | rs17066096 |
| ebi | rs17066096 |
| HLI | rs17066096 |
| Exac | rs17066096 |
| Gnomad | rs17066096 |
| Varsome | rs17066096 |
| LitVar | rs17066096 |
| Map | rs17066096 |
| PheGenI | rs17066096 |
| Biobank | rs17066096 |
| 1000 genomes | rs17066096 |
| hgdp | rs17066096 |
| ensembl | rs17066096 |
| geneview | rs17066096 |
| scholar | rs17066096 |
| rs17066096 | |
| pharmgkb | rs17066096 |
| gwascentral | rs17066096 |
| openSNP | rs17066096 |
| 23andMe | rs17066096 |
| SNPshot | rs17066096 |
| SNPdbe | rs17066096 |
| MSV3d | rs17066096 |
| GWAS Ctlg | rs17066096 |
| GMAF | 0.1722 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
23andMe blog multiple sclerosis rs17066096 IL22RA2 G 1.14
| GWAS snp | |
|---|---|
| PMID | [PMID 21833088 ]
|
| Trait | |
| Title | Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. |
| Risk Allele | G |
| P-val | 6E-13 |
| Odds Ratio | 1.1400 [1.12-1.15] |
[PMID 31936765] The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis.
