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rs2834215

From SNPedia

Orientationplus
Stabilizedplus
Make rs2834215(A;A)
Make rs2834215(A;G)
Make rs2834215(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position33424579
GeneIFNGR2
is asnp
is mentioned by
dbSNPrs2834215
ebirs2834215
HLIrs2834215
Exacrs2834215
Varsomers2834215
Maprs2834215
PheGenIrs2834215
hapmaprs2834215
1000 genomesrs2834215
hgdprs2834215
ensemblrs2834215
gopubmedrs2834215
geneviewrs2834215
scholarrs2834215
googlers2834215
pharmgkbrs2834215
gwascentralrs2834215
openSNPrs2834215
23andMers2834215
23andMe allrs2834215
SNP Nexus

SNPshotrs2834215
SNPdbers2834215
MSV3drs2834215
GWAS Ctlgrs2834215
GMAF0.3825
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22936669]
Trait Crohn's disease
Title A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.
Risk Allele
P-val 3E-7
Odds Ratio 1.22 [1.12-1.32]