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