rs918629
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs918629(A;A) |
Make rs918629(A;G) |
Make rs918629(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 95965759 |
Gene | LOC101929710 |
is a | snp |
is | mentioned by |
dbSNP | rs918629 |
dbSNP (classic) | rs918629 |
ClinGen | rs918629 |
ebi | rs918629 |
HLI | rs918629 |
Exac | rs918629 |
Gnomad | rs918629 |
Varsome | rs918629 |
LitVar | rs918629 |
Map | rs918629 |
PheGenI | rs918629 |
Biobank | rs918629 |
1000 genomes | rs918629 |
hgdp | rs918629 |
ensembl | rs918629 |
geneview | rs918629 |
scholar | rs918629 |
rs918629 | |
pharmgkb | rs918629 |
gwascentral | rs918629 |
openSNP | rs918629 |
23andMe | rs918629 |
SNPshot | rs918629 |
SNPdbe | rs918629 |
MSV3d | rs918629 |
GWAS Ctlg | rs918629 |
GMAF | 0.4894 |
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 | 1E-6 |
Odds Ratio | .17 [0.1-0.24] unit increase |