rs255982
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs255982(C;C) |
Make rs255982(C;T) |
Make rs255982(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 95318169 |
is a | snp |
is | mentioned by |
dbSNP | rs255982 |
dbSNP (classic) | rs255982 |
ClinGen | rs255982 |
ebi | rs255982 |
HLI | rs255982 |
Exac | rs255982 |
Gnomad | rs255982 |
Varsome | rs255982 |
LitVar | rs255982 |
Map | rs255982 |
PheGenI | rs255982 |
Biobank | rs255982 |
1000 genomes | rs255982 |
hgdp | rs255982 |
ensembl | rs255982 |
geneview | rs255982 |
scholar | rs255982 |
rs255982 | |
pharmgkb | rs255982 |
gwascentral | rs255982 |
openSNP | rs255982 |
23andMe | rs255982 |
SNPshot | rs255982 |
SNPdbe | rs255982 |
MSV3d | rs255982 |
GWAS Ctlg | rs255982 |
GMAF | 0.08861 |
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 | G |
P-val | 8E-6 |
Odds Ratio | .21 [0.12-0.3] unit increase |