rs4917017
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4917017(A;A) |
| Make rs4917017(A;G) |
| Make rs4917017(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 50295636 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4917017 |
| dbSNP (classic) | rs4917017 |
| ClinGen | rs4917017 |
| ebi | rs4917017 |
| HLI | rs4917017 |
| Exac | rs4917017 |
| Gnomad | rs4917017 |
| Varsome | rs4917017 |
| LitVar | rs4917017 |
| Map | rs4917017 |
| PheGenI | rs4917017 |
| Biobank | rs4917017 |
| 1000 genomes | rs4917017 |
| hgdp | rs4917017 |
| ensembl | rs4917017 |
| geneview | rs4917017 |
| scholar | rs4917017 |
| rs4917017 | |
| pharmgkb | rs4917017 |
| gwascentral | rs4917017 |
| openSNP | rs4917017 |
| 23andMe | rs4917017 |
| SNPshot | rs4917017 |
| SNPdbe | rs4917017 |
| MSV3d | rs4917017 |
| GWAS Ctlg | rs4917017 |
| GMAF | 0.3687 |
| 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 | G |
| P-val | 1E-8 |
| Odds Ratio | .20 [0.13-0.27] unit increase |
