rs17594709
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17594709(A;A) |
Make rs17594709(A;G) |
Make rs17594709(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 12179909 |
is a | snp |
is | mentioned by |
dbSNP | rs17594709 |
dbSNP (classic) | rs17594709 |
ClinGen | rs17594709 |
ebi | rs17594709 |
HLI | rs17594709 |
Exac | rs17594709 |
Gnomad | rs17594709 |
Varsome | rs17594709 |
LitVar | rs17594709 |
Map | rs17594709 |
PheGenI | rs17594709 |
Biobank | rs17594709 |
1000 genomes | rs17594709 |
hgdp | rs17594709 |
ensembl | rs17594709 |
geneview | rs17594709 |
scholar | rs17594709 |
rs17594709 | |
pharmgkb | rs17594709 |
gwascentral | rs17594709 |
openSNP | rs17594709 |
23andMe | rs17594709 |
SNPshot | rs17594709 |
SNPdbe | rs17594709 |
MSV3d | rs17594709 |
GWAS Ctlg | rs17594709 |
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 | .16 [0.09-0.225] unit decrease |