Have questions? Visit https://www.reddit.com/r/SNPedia

rs2284553

From SNPedia

Orientationplus
Stabilizedplus
Make rs2284553(A;A)
Make rs2284553(A;G)
Make rs2284553(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position33404389
GeneIFNGR2
is asnp
is mentioned by
dbSNPrs2284553
ebirs2284553
HLIrs2284553
Exacrs2284553
Varsomers2284553
Maprs2284553
PheGenIrs2284553
hapmaprs2284553
1000 genomesrs2284553
hgdprs2284553
ensemblrs2284553
gopubmedrs2284553
geneviewrs2284553
scholarrs2284553
googlers2284553
pharmgkbrs2284553
gwascentralrs2284553
openSNPrs2284553
23andMers2284553
23andMe allrs2284553
SNP Nexus

SNPshotrs2284553
SNPdbers2284553
MSV3drs2284553
GWAS Ctlgrs2284553
GMAF0.3058
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23128233OA-icon.png]
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.