rs4866334
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4866334(C;C) |
Make rs4866334(C;T) |
Make rs4866334(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 18483542 |
is a | snp |
is | mentioned by |
dbSNP | rs4866334 |
dbSNP (classic) | rs4866334 |
ClinGen | rs4866334 |
ebi | rs4866334 |
HLI | rs4866334 |
Exac | rs4866334 |
Gnomad | rs4866334 |
Varsome | rs4866334 |
LitVar | rs4866334 |
Map | rs4866334 |
PheGenI | rs4866334 |
Biobank | rs4866334 |
1000 genomes | rs4866334 |
hgdp | rs4866334 |
ensembl | rs4866334 |
geneview | rs4866334 |
scholar | rs4866334 |
rs4866334 | |
pharmgkb | rs4866334 |
gwascentral | rs4866334 |
openSNP | rs4866334 |
23andMe | rs4866334 |
SNPshot | rs4866334 |
SNPdbe | rs4866334 |
MSV3d | rs4866334 |
GWAS Ctlg | rs4866334 |
GMAF | 0.08494 |
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 | .25 [0.15-0.36] unit decrease |