rs7700895
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7700895(A;A) |
Make rs7700895(A;T) |
Make rs7700895(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 95937706 |
Gene | ELL2 |
is a | snp |
is | mentioned by |
dbSNP | rs7700895 |
dbSNP (classic) | rs7700895 |
ClinGen | rs7700895 |
ebi | rs7700895 |
HLI | rs7700895 |
Exac | rs7700895 |
Gnomad | rs7700895 |
Varsome | rs7700895 |
LitVar | rs7700895 |
Map | rs7700895 |
PheGenI | rs7700895 |
Biobank | rs7700895 |
1000 genomes | rs7700895 |
hgdp | rs7700895 |
ensembl | rs7700895 |
geneview | rs7700895 |
scholar | rs7700895 |
rs7700895 | |
pharmgkb | rs7700895 |
gwascentral | rs7700895 |
openSNP | rs7700895 |
23andMe | rs7700895 |
SNPshot | rs7700895 |
SNPdbe | rs7700895 |
MSV3d | rs7700895 |
GWAS Ctlg | rs7700895 |
GMAF | 0.3696 |
Max Magnitude | 0 |
? | (A;A) (A;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 | T |
P-val | 1E-6 |
Odds Ratio | .18 [0.11-0.25] unit decrease |