rs2514895
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2514895(C;C) |
Make rs2514895(C;T) |
Make rs2514895(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 127240288 |
is a | snp |
is | mentioned by |
dbSNP | rs2514895 |
dbSNP (classic) | rs2514895 |
ClinGen | rs2514895 |
ebi | rs2514895 |
HLI | rs2514895 |
Exac | rs2514895 |
Gnomad | rs2514895 |
Varsome | rs2514895 |
LitVar | rs2514895 |
Map | rs2514895 |
PheGenI | rs2514895 |
Biobank | rs2514895 |
1000 genomes | rs2514895 |
hgdp | rs2514895 |
ensembl | rs2514895 |
geneview | rs2514895 |
scholar | rs2514895 |
rs2514895 | |
pharmgkb | rs2514895 |
gwascentral | rs2514895 |
openSNP | rs2514895 |
23andMe | rs2514895 |
SNPshot | rs2514895 |
SNPdbe | rs2514895 |
MSV3d | rs2514895 |
GWAS Ctlg | rs2514895 |
GMAF | 0.3577 |
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 | 2E-6 |
Odds Ratio | .19 [0.11-0.26] unit decrease |