rs4869266
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4869266(A;A) |
Make rs4869266(A;G) |
Make rs4869266(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 96151236 |
Gene | LOC101929710, LOC107984114 |
is a | snp |
is | mentioned by |
dbSNP | rs4869266 |
dbSNP (classic) | rs4869266 |
ClinGen | rs4869266 |
ebi | rs4869266 |
HLI | rs4869266 |
Exac | rs4869266 |
Gnomad | rs4869266 |
Varsome | rs4869266 |
LitVar | rs4869266 |
Map | rs4869266 |
PheGenI | rs4869266 |
Biobank | rs4869266 |
1000 genomes | rs4869266 |
hgdp | rs4869266 |
ensembl | rs4869266 |
geneview | rs4869266 |
scholar | rs4869266 |
rs4869266 | |
pharmgkb | rs4869266 |
gwascentral | rs4869266 |
openSNP | rs4869266 |
23andMe | rs4869266 |
SNPshot | rs4869266 |
SNPdbe | rs4869266 |
MSV3d | rs4869266 |
GWAS Ctlg | rs4869266 |
GMAF | 0.3783 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | G |
P-val | 3E-6 |
Odds Ratio | .15 [0.088-0.216] unit increase |