rs12950390
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12950390(C;C) |
Make rs12950390(C;T) |
Make rs12950390(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 47753582 |
is a | snp |
is | mentioned by |
dbSNP | rs12950390 |
dbSNP (classic) | rs12950390 |
ClinGen | rs12950390 |
ebi | rs12950390 |
HLI | rs12950390 |
Exac | rs12950390 |
Gnomad | rs12950390 |
Varsome | rs12950390 |
LitVar | rs12950390 |
Map | rs12950390 |
PheGenI | rs12950390 |
Biobank | rs12950390 |
1000 genomes | rs12950390 |
hgdp | rs12950390 |
ensembl | rs12950390 |
geneview | rs12950390 |
scholar | rs12950390 |
rs12950390 | |
pharmgkb | rs12950390 |
gwascentral | rs12950390 |
openSNP | rs12950390 |
23andMe | rs12950390 |
SNPshot | rs12950390 |
SNPdbe | rs12950390 |
MSV3d | rs12950390 |
GWAS Ctlg | rs12950390 |
GMAF | 0.2066 |
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 | 3E-6 |
Odds Ratio | .17 [0.098-0.239] unit decrease |