rs10751776
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10751776(A;A) |
| Make rs10751776(A;C) |
| Make rs10751776(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 24970252 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10751776 |
| dbSNP (classic) | rs10751776 |
| ClinGen | rs10751776 |
| ebi | rs10751776 |
| HLI | rs10751776 |
| Exac | rs10751776 |
| Gnomad | rs10751776 |
| Varsome | rs10751776 |
| LitVar | rs10751776 |
| Map | rs10751776 |
| PheGenI | rs10751776 |
| Biobank | rs10751776 |
| 1000 genomes | rs10751776 |
| hgdp | rs10751776 |
| ensembl | rs10751776 |
| geneview | rs10751776 |
| scholar | rs10751776 |
| rs10751776 | |
| pharmgkb | rs10751776 |
| gwascentral | rs10751776 |
| openSNP | rs10751776 |
| 23andMe | rs10751776 |
| SNPshot | rs10751776 |
| SNPdbe | rs10751776 |
| MSV3d | rs10751776 |
| GWAS Ctlg | rs10751776 |
| GMAF | 0.3379 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 7E-6 |
| Odds Ratio | .15 [0.084-0.213] unit increase |
