rs4789580
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4789580(A;A) |
Make rs4789580(A;C) |
Make rs4789580(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 78315910 |
is a | snp |
is | mentioned by |
dbSNP | rs4789580 |
dbSNP (classic) | rs4789580 |
ClinGen | rs4789580 |
ebi | rs4789580 |
HLI | rs4789580 |
Exac | rs4789580 |
Gnomad | rs4789580 |
Varsome | rs4789580 |
LitVar | rs4789580 |
Map | rs4789580 |
PheGenI | rs4789580 |
Biobank | rs4789580 |
1000 genomes | rs4789580 |
hgdp | rs4789580 |
ensembl | rs4789580 |
geneview | rs4789580 |
scholar | rs4789580 |
rs4789580 | |
pharmgkb | rs4789580 |
gwascentral | rs4789580 |
openSNP | rs4789580 |
23andMe | rs4789580 |
SNPshot | rs4789580 |
SNPdbe | rs4789580 |
MSV3d | rs4789580 |
GWAS Ctlg | rs4789580 |
GMAF | 0.3333 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 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 | 9E-6 |
Odds Ratio | .23 [0.13-0.33] unit increase |