rs2200578
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2200578(C;C) |
Make rs2200578(C;T) |
Make rs2200578(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 99259781 |
is a | snp |
is | mentioned by |
dbSNP | rs2200578 |
dbSNP (classic) | rs2200578 |
ClinGen | rs2200578 |
ebi | rs2200578 |
HLI | rs2200578 |
Exac | rs2200578 |
Gnomad | rs2200578 |
Varsome | rs2200578 |
LitVar | rs2200578 |
Map | rs2200578 |
PheGenI | rs2200578 |
Biobank | rs2200578 |
1000 genomes | rs2200578 |
hgdp | rs2200578 |
ensembl | rs2200578 |
geneview | rs2200578 |
scholar | rs2200578 |
rs2200578 | |
pharmgkb | rs2200578 |
gwascentral | rs2200578 |
openSNP | rs2200578 |
23andMe | rs2200578 |
SNPshot | rs2200578 |
SNPdbe | rs2200578 |
MSV3d | rs2200578 |
GWAS Ctlg | rs2200578 |
GMAF | 0.208 |
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 | 4E-7 |
Odds Ratio | .19 [0.12-0.26] unit decrease |