rs137699
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs137699(A;A) |
| Make rs137699(A;G) |
| Make rs137699(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 39352849 |
| Gene | SYNGR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs137699 |
| dbSNP (classic) | rs137699 |
| ClinGen | rs137699 |
| ebi | rs137699 |
| HLI | rs137699 |
| Exac | rs137699 |
| Gnomad | rs137699 |
| Varsome | rs137699 |
| LitVar | rs137699 |
| Map | rs137699 |
| PheGenI | rs137699 |
| Biobank | rs137699 |
| 1000 genomes | rs137699 |
| hgdp | rs137699 |
| ensembl | rs137699 |
| geneview | rs137699 |
| scholar | rs137699 |
| rs137699 | |
| pharmgkb | rs137699 |
| gwascentral | rs137699 |
| openSNP | rs137699 |
| 23andMe | rs137699 |
| SNPshot | rs137699 |
| SNPdbe | rs137699 |
| MSV3d | rs137699 |
| GWAS Ctlg | rs137699 |
| GMAF | 0.3701 |
| 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 | 8E-6 |
| Odds Ratio | .16 [0.088-0.225] unit decrease |
