rs2163237
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2163237(A;A) |
Make rs2163237(A;G) |
Make rs2163237(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 55746597 |
is a | snp |
is | mentioned by |
dbSNP | rs2163237 |
dbSNP (classic) | rs2163237 |
ClinGen | rs2163237 |
ebi | rs2163237 |
HLI | rs2163237 |
Exac | rs2163237 |
Gnomad | rs2163237 |
Varsome | rs2163237 |
LitVar | rs2163237 |
Map | rs2163237 |
PheGenI | rs2163237 |
Biobank | rs2163237 |
1000 genomes | rs2163237 |
hgdp | rs2163237 |
ensembl | rs2163237 |
geneview | rs2163237 |
scholar | rs2163237 |
rs2163237 | |
pharmgkb | rs2163237 |
gwascentral | rs2163237 |
openSNP | rs2163237 |
23andMe | rs2163237 |
SNPshot | rs2163237 |
SNPdbe | rs2163237 |
MSV3d | rs2163237 |
GWAS Ctlg | rs2163237 |
GMAF | 0.4017 |
Max Magnitude | 0 |
? | (A;A) (A;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 | 5E-6 |
Odds Ratio | .15 [0.087-0.217] unit decrease |