rs12600635
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs12600635(A;A) |
| Make rs12600635(A;G) |
| Make rs12600635(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 17239582 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs12600635 |
| dbSNP (classic) | rs12600635 |
| ClinGen | rs12600635 |
| ebi | rs12600635 |
| HLI | rs12600635 |
| Exac | rs12600635 |
| Gnomad | rs12600635 |
| Varsome | rs12600635 |
| LitVar | rs12600635 |
| Map | rs12600635 |
| PheGenI | rs12600635 |
| Biobank | rs12600635 |
| 1000 genomes | rs12600635 |
| hgdp | rs12600635 |
| ensembl | rs12600635 |
| geneview | rs12600635 |
| scholar | rs12600635 |
| rs12600635 | |
| pharmgkb | rs12600635 |
| gwascentral | rs12600635 |
| openSNP | rs12600635 |
| 23andMe | rs12600635 |
| SNPshot | rs12600635 |
| SNPdbe | rs12600635 |
| MSV3d | rs12600635 |
| GWAS Ctlg | rs12600635 |
| GMAF | 0.1589 |
| 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 | 2E-7 |
| Odds Ratio | .23 [0.14-0.31] unit decrease |
