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rs3897478

From SNPedia

Orientationplus
Stabilizedplus
Make rs3897478(C;C)
Make rs3897478(C;T)
Make rs3897478(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position119908567
is asnp
is mentioned by
dbSNPrs3897478
ebirs3897478
HLIrs3897478
Exacrs3897478
Varsomers3897478
Maprs3897478
PheGenIrs3897478
hapmaprs3897478
1000 genomesrs3897478
hgdprs3897478
ensemblrs3897478
gopubmedrs3897478
geneviewrs3897478
scholarrs3897478
googlers3897478
pharmgkbrs3897478
gwascentralrs3897478
openSNPrs3897478
23andMers3897478
23andMe allrs3897478
SNP Nexus

SNPshotrs3897478
SNPdbers3897478
MSV3drs3897478
GWAS Ctlgrs3897478
GMAF0.1534
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 2E-11
Odds Ratio 1.16 [1.101-1.224]