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rs4820425

From SNPedia

Orientationplus
Stabilizedplus
Make rs4820425(A;A)
Make rs4820425(A;C)
Make rs4820425(C;C)
ReferenceGRCh38 38.1/141
Chromosome22
Position41035338
is asnp
is mentioned by
dbSNPrs4820425
ebirs4820425
HLIrs4820425
Exacrs4820425
Varsomers4820425
Maprs4820425
PheGenIrs4820425
hapmaprs4820425
1000 genomesrs4820425
hgdprs4820425
ensemblrs4820425
gopubmedrs4820425
geneviewrs4820425
scholarrs4820425
googlers4820425
pharmgkbrs4820425
gwascentralrs4820425
openSNPrs4820425
23andMers4820425
23andMe allrs4820425
SNP Nexus

SNPshotrs4820425
SNPdbers4820425
MSV3drs4820425
GWAS Ctlgrs4820425
GMAF0.2383
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 3E-8
Odds Ratio 1.27 [1.17-1.38]