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

rs4871611

From SNPedia

Orientationplus
Stabilizedplus
Make rs4871611(A;A)
Make rs4871611(A;G)
Make rs4871611(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position125525328
is asnp
is mentioned by
dbSNPrs4871611
ebirs4871611
HLIrs4871611
Exacrs4871611
Varsomers4871611
Maprs4871611
PheGenIrs4871611
hapmaprs4871611
1000 genomesrs4871611
hgdprs4871611
ensemblrs4871611
gopubmedrs4871611
geneviewrs4871611
scholarrs4871611
googlers4871611
pharmgkbrs4871611
gwascentralrs4871611
openSNPrs4871611
23andMers4871611
23andMe allrs4871611
SNP Nexus

SNPshotrs4871611
SNPdbers4871611
MSV3drs4871611
GWAS Ctlgrs4871611
GMAF0.4307
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait Crohn's disease
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
Risk Allele A
P-val 2E-12
Odds Ratio 1.17 [1.12-1.23]