rs11581667
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11581667(C;C) |
Make rs11581667(C;T) |
Make rs11581667(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 234590610 |
is a | snp |
is | mentioned by |
dbSNP | rs11581667 |
dbSNP (classic) | rs11581667 |
ClinGen | rs11581667 |
ebi | rs11581667 |
HLI | rs11581667 |
Exac | rs11581667 |
Gnomad | rs11581667 |
Varsome | rs11581667 |
LitVar | rs11581667 |
Map | rs11581667 |
PheGenI | rs11581667 |
Biobank | rs11581667 |
1000 genomes | rs11581667 |
hgdp | rs11581667 |
ensembl | rs11581667 |
geneview | rs11581667 |
scholar | rs11581667 |
rs11581667 | |
pharmgkb | rs11581667 |
gwascentral | rs11581667 |
openSNP | rs11581667 |
23andMe | rs11581667 |
SNPshot | rs11581667 |
SNPdbe | rs11581667 |
MSV3d | rs11581667 |
GWAS Ctlg | rs11581667 |
GMAF | 0.2727 |
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 | 4E-6 |
Odds Ratio | .20 [0.11-0.28] unit increase |