rs1049110
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1049110(A;A) |
| Make rs1049110(A;G) |
| Make rs1049110(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32759026 |
| Gene | HLA-DQB2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1049110 |
| dbSNP (classic) | rs1049110 |
| ClinGen | rs1049110 |
| ebi | rs1049110 |
| HLI | rs1049110 |
| Exac | rs1049110 |
| Gnomad | rs1049110 |
| Varsome | rs1049110 |
| LitVar | rs1049110 |
| Map | rs1049110 |
| PheGenI | rs1049110 |
| Biobank | rs1049110 |
| 1000 genomes | rs1049110 |
| hgdp | rs1049110 |
| ensembl | rs1049110 |
| geneview | rs1049110 |
| scholar | rs1049110 |
| rs1049110 | |
| pharmgkb | rs1049110 |
| gwascentral | rs1049110 |
| openSNP | rs1049110 |
| 23andMe | rs1049110 |
| SNPshot | rs1049110 |
| SNPdbe | rs1049110 |
| MSV3d | rs1049110 |
| GWAS Ctlg | rs1049110 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23382691 ]
|
| Trait | IgG glycosylation |
| Title | Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. |
| Risk Allele | C |
| P-val | 4E8 |
| Odds Ratio | .19 [0.12-0.25] unit increase |
[PMID 19143815] MHC fine mapping of human type 1 diabetes using the T1DGC data.
