rs2189812
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2189812(C;C) |
Make rs2189812(C;G) |
Make rs2189812(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 86719683 |
Gene | GRM3 |
is a | snp |
is | mentioned by |
dbSNP | rs2189812 |
dbSNP (classic) | rs2189812 |
ClinGen | rs2189812 |
ebi | rs2189812 |
HLI | rs2189812 |
Exac | rs2189812 |
Gnomad | rs2189812 |
Varsome | rs2189812 |
LitVar | rs2189812 |
Map | rs2189812 |
PheGenI | rs2189812 |
Biobank | rs2189812 |
1000 genomes | rs2189812 |
hgdp | rs2189812 |
ensembl | rs2189812 |
geneview | rs2189812 |
scholar | rs2189812 |
rs2189812 | |
pharmgkb | rs2189812 |
gwascentral | rs2189812 |
openSNP | rs2189812 |
23andMe | rs2189812 |
SNPshot | rs2189812 |
SNPdbe | rs2189812 |
MSV3d | rs2189812 |
GWAS Ctlg | rs2189812 |
GMAF | 0.146 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 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 | 6E-6 |
Odds Ratio | .16 [0.092-0.233] unit increase |