rs2284553
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2284553(A;A) |
Make rs2284553(A;G) |
Make rs2284553(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 33404389 |
Gene | IFNGR2 |
is a | snp |
is | mentioned by |
dbSNP | rs2284553 |
dbSNP (classic) | rs2284553 |
ClinGen | rs2284553 |
ebi | rs2284553 |
HLI | rs2284553 |
Exac | rs2284553 |
Gnomad | rs2284553 |
Varsome | rs2284553 |
LitVar | rs2284553 |
Map | rs2284553 |
PheGenI | rs2284553 |
Biobank | rs2284553 |
1000 genomes | rs2284553 |
hgdp | rs2284553 |
ensembl | rs2284553 |
geneview | rs2284553 |
scholar | rs2284553 |
rs2284553 | |
pharmgkb | rs2284553 |
gwascentral | rs2284553 |
openSNP | rs2284553 |
23andMe | rs2284553 |
SNPshot | rs2284553 |
SNPdbe | rs2284553 |
MSV3d | rs2284553 |
GWAS Ctlg | rs2284553 |
GMAF | 0.3058 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23128233] |
Trait | Crohn's disease |
Title | Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. |
Risk Allele | G |
P-val | 2E-16 |
Odds Ratio | 1.12 [1.086-1.162] |
[PMID 20980339] Hepatitis B viraemia: its heritability and association with common genetic variation in the interferon gamma signalling pathway.