rs11079764
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11079764(A;A) |
Make rs11079764(A;G) |
Make rs11079764(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 47232327 |
is a | snp |
is | mentioned by |
dbSNP | rs11079764 |
dbSNP (classic) | rs11079764 |
ClinGen | rs11079764 |
ebi | rs11079764 |
HLI | rs11079764 |
Exac | rs11079764 |
Gnomad | rs11079764 |
Varsome | rs11079764 |
LitVar | rs11079764 |
Map | rs11079764 |
PheGenI | rs11079764 |
Biobank | rs11079764 |
1000 genomes | rs11079764 |
hgdp | rs11079764 |
ensembl | rs11079764 |
geneview | rs11079764 |
scholar | rs11079764 |
rs11079764 | |
pharmgkb | rs11079764 |
gwascentral | rs11079764 |
openSNP | rs11079764 |
23andMe | rs11079764 |
SNPshot | rs11079764 |
SNPdbe | rs11079764 |
MSV3d | rs11079764 |
GWAS Ctlg | rs11079764 |
GMAF | 0.3802 |
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 | 5E-6 |
Odds Ratio | .18 [0.1-0.26] unit decrease |