rs1039443
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1039443(C;C) |
| Make rs1039443(C;T) |
| Make rs1039443(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 16037993 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1039443 |
| dbSNP (classic) | rs1039443 |
| ClinGen | rs1039443 |
| ebi | rs1039443 |
| HLI | rs1039443 |
| Exac | rs1039443 |
| Gnomad | rs1039443 |
| Varsome | rs1039443 |
| LitVar | rs1039443 |
| Map | rs1039443 |
| PheGenI | rs1039443 |
| Biobank | rs1039443 |
| 1000 genomes | rs1039443 |
| hgdp | rs1039443 |
| ensembl | rs1039443 |
| geneview | rs1039443 |
| scholar | rs1039443 |
| rs1039443 | |
| pharmgkb | rs1039443 |
| gwascentral | rs1039443 |
| openSNP | rs1039443 |
| 23andMe | rs1039443 |
| SNPshot | rs1039443 |
| SNPdbe | rs1039443 |
| MSV3d | rs1039443 |
| GWAS Ctlg | rs1039443 |
| GMAF | 0.1676 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 8E-6 |
| Odds Ratio | .22 [0.12-0.32] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 5
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
