rs10069748
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10069748(C;C) |
Make rs10069748(C;T) |
Make rs10069748(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 95905518 |
Gene | ELL2 |
is a | snp |
is | mentioned by |
dbSNP | rs10069748 |
dbSNP (classic) | rs10069748 |
ClinGen | rs10069748 |
ebi | rs10069748 |
HLI | rs10069748 |
Exac | rs10069748 |
Gnomad | rs10069748 |
Varsome | rs10069748 |
LitVar | rs10069748 |
Map | rs10069748 |
PheGenI | rs10069748 |
Biobank | rs10069748 |
1000 genomes | rs10069748 |
hgdp | rs10069748 |
ensembl | rs10069748 |
geneview | rs10069748 |
scholar | rs10069748 |
rs10069748 | |
pharmgkb | rs10069748 |
gwascentral | rs10069748 |
openSNP | rs10069748 |
23andMe | rs10069748 |
SNPshot | rs10069748 |
SNPdbe | rs10069748 |
MSV3d | rs10069748 |
GWAS Ctlg | rs10069748 |
GMAF | 0.4132 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 5E-6 |
Odds Ratio | .15 [0.088-0.22] unit decrease |