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rs16967103

From SNPedia

Orientationplus
Stabilizedplus
Make rs16967103(C;C)
Make rs16967103(C;T)
Make rs16967103(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position38606989
is asnp
is mentioned by
dbSNPrs16967103
ebirs16967103
HLIrs16967103
Exacrs16967103
Varsomers16967103
Maprs16967103
PheGenIrs16967103
hapmaprs16967103
1000 genomesrs16967103
hgdprs16967103
ensemblrs16967103
gopubmedrs16967103
geneviewrs16967103
scholarrs16967103
googlers16967103
pharmgkbrs16967103
gwascentralrs16967103
openSNPrs16967103
23andMers16967103
23andMe allrs16967103
SNP Nexus

SNPshotrs16967103
SNPdbers16967103
MSV3drs16967103
GWAS Ctlgrs16967103
GMAF0.1593
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 C
P-val 4E-9
Odds Ratio 1.09 [1.045-1.132]