rs16949825
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16949825(C;C) |
Make rs16949825(C;G) |
Make rs16949825(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 48701073 |
Gene | CTIF |
is a | snp |
is | mentioned by |
dbSNP | rs16949825 |
dbSNP (classic) | rs16949825 |
ClinGen | rs16949825 |
ebi | rs16949825 |
HLI | rs16949825 |
Exac | rs16949825 |
Gnomad | rs16949825 |
Varsome | rs16949825 |
LitVar | rs16949825 |
Map | rs16949825 |
PheGenI | rs16949825 |
Biobank | rs16949825 |
1000 genomes | rs16949825 |
hgdp | rs16949825 |
ensembl | rs16949825 |
geneview | rs16949825 |
scholar | rs16949825 |
rs16949825 | |
pharmgkb | rs16949825 |
gwascentral | rs16949825 |
openSNP | rs16949825 |
23andMe | rs16949825 |
SNPshot | rs16949825 |
SNPdbe | rs16949825 |
MSV3d | rs16949825 |
GWAS Ctlg | rs16949825 |
GMAF | 0.112 |
Max Magnitude | 0 |
? | (C;C) (C;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 | C |
P-val | 7E-6 |
Odds Ratio | .25 [0.14-0.35] unit increase |