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rs1869839

From SNPedia

Orientationplus
Stabilizedplus
Make rs1869839(A;A)
Make rs1869839(A;G)
Make rs1869839(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position114717488
is asnp
is mentioned by
dbSNPrs1869839
ebirs1869839
HLIrs1869839
Exacrs1869839
Varsomers1869839
Maprs1869839
PheGenIrs1869839
hapmaprs1869839
1000 genomesrs1869839
hgdprs1869839
ensemblrs1869839
gopubmedrs1869839
geneviewrs1869839
scholarrs1869839
googlers1869839
pharmgkbrs1869839
gwascentralrs1869839
openSNPrs1869839
23andMers1869839
23andMe allrs1869839
SNP Nexus

SNPshotrs1869839
SNPdbers1869839
MSV3drs1869839
GWAS Ctlgrs1869839
GMAF0.2089
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 7E-6
Odds Ratio 1.20 [1.11-1.3]